MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS— 510(k) K801880

Name: FDA 510(k) clearance K801880
Creator: U.S. Food and Drug Administration
Published: 1980-08-14

Substantially Equivalent

Medical Measurements, Inc.

FDA 510(k) clearance K801880 for MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS, Substantially Equivalent on 1980-08-14. Applicant: Medical Measurements, Inc.. Device class: 1.

Clearance details

Applicant: Medical Measurements, Inc.
Product code: Code BYR
Device class: Class 1
Regulation: 21 CFR 868.2875
Advisory panel: Anesthesiology
Date received: 1980-08-07
Decision date: 1980-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K801757 — MMI/GAELTEC CATHETER TIP PRESS. TRANSDU1980-08-27
K801756 — MMI/GAELTEC CATHETER TIP TRANSDUC1980-08-20

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