MMI/GAELTEC CATHETER TIP PRESS. TRANSDU— 510(k) K801757

Name: FDA 510(k) clearance K801757
Creator: U.S. Food and Drug Administration
Published: 1980-08-27

Substantially Equivalent

Medical Measurements, Inc.

FDA 510(k) clearance K801757 for MMI/GAELTEC CATHETER TIP PRESS. TRANSDU, Substantially Equivalent on 1980-08-27. Applicant: Medical Measurements, Inc.. Device class: 2.

Clearance details

Applicant: Medical Measurements, Inc.
Product code: Code FES
Device class: Class 2
Regulation: 21 CFR 876.1725
Advisory panel: Gastroenterology, Urology
Date received: 1980-07-28
Decision date: 1980-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K863479 — MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL1986-10-14
K801756 — MMI/GAELTEC CATHETER TIP TRANSDUC1980-08-20
K801758 — MMI/GAELTEC CATHETER INTRAUTERINE1980-08-14

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