MICRO MEDICAL SOLUTIONS INC

FDA Device Registration & Listing · Woburn, MA, US · Registration 3013391155

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013391155
FEI Number
3013391155
Entity Name
MICRO MEDICAL SOLUTIONS INC
City/State/Country
Woburn, MA, US
Establishment Address
175 New Boston St Ste H, Woburn, MA 01801, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Micro Medical Solutions Inc (Owner Number: 10059633)
Owner / Operator Contact Address
175 New Boston Street, Suite H, Woburn, MA 01801, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MicroGuide MicroBalloon

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KRA Catheter, Continuous Flush Cardiovascular Class 2 870.1210 2019-02-05
LIT Catheter, Angioplasty, Peripheral, Transluminal Cardiovascular Class 2 870.1250 2019-02-05

Official Correspondent

Greg Mathison

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Micro Medical Solutions Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K792141 Pharmaseal Div., Baxter Healthcare Corp. CONTINUOUS FLUSH DEVICE 1979-12-05
K924661 Baxter Healthcare Corp SWAN-GANZ INTELLICATH CCO THERMODILUTION CATHETER 1993-04-08
K171251 Creagh Medical 014 Hydrophilic Coated PTA Balloon Dilatation Catheter 2017-09-08
K103464 Medtronic, Inc. PACIFIC XTREME PTCA BALLOON DILATATION CATHETER 2010-12-22
K252512 ABBOTT MEDICAL Armada™ 14 NC PTA Catheter 2026-02-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013391155. Last updated year: 2026. Please use registration number 3013391155 when referencing this establishment in official correspondence.
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