MODEL 5000 MICROMANIPULATOR MICRO CO2 LASER SYSTEM

FDA 510(k) Premarket Notification · Submission K870161 · Applicant: Coherent Medical Group

Public Record 510(k) Submission Decision Date: 1987-04-14 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K870161.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K870161
Applicant / Sponsor
Device Name
MODEL 5000 MICROMANIPULATOR MICRO CO2 LASER SYSTEM
Product Code
GEX
Decision Date
1987-04-14
Decision / Status
Substantially Equivalent for Some Indications (SN)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1987-01-13

Related Establishments / Registrations

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