MODEL 412 ELECTROFLUIDIC MANOMETER

FDA 510(k) Premarket Notification · Submission K800222 · Applicant: Med-Tek Corp.

Public Record 510(k) Submission Decision Date: 1980-02-29 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K800222.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K800222

Applicant / Sponsor

Med-Tek Corp.

Device Name

MODEL 412 ELECTROFLUIDIC MANOMETER

Product Code

DXW

Decision Date

1980-02-29

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Traditional

Third Party Flag

Date Received

1980-02-04

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.