MAXI-VAC TM— 510(k) K790763

Name: FDA 510(k) clearance K790763
Creator: U.S. Food and Drug Administration
Published: 1979-04-23

Substantially Equivalent

Med General

FDA 510(k) clearance K790763 for MAXI-VAC TM, Substantially Equivalent on 1979-04-23. Applicant: Med General. Device class: 1.

Clearance details

Applicant: Med General
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1979-04-18
Decision date: 1979-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Med General

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K791097 — CEPTORTRODE WITH CEPTOR HESIVE1979-08-03
K791098 — SINGLE-USE MINI-BULLDOG1979-06-22
K790269 — CEPTOR HESIVE1979-02-26
K782006 — MEDGENERAL SINGLE-USE BULLDOG1978-12-15
K781239 — MYO-STIM1978-11-03

Adverse events under product code GCY

product code GCY

Malfunction: 786
Other: 1
Total: 787

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.