MOGAN CIRCUMCISION CLAMP— 510(k) K926471

Name: FDA 510(k) clearance K926471
Creator: U.S. Food and Drug Administration
Published: 1994-02-25

Substantially Equivalent

Thomasville Medical Assoc.

FDA 510(k) clearance K926471 for MOGAN CIRCUMCISION CLAMP, Substantially Equivalent on 1994-02-25. Applicant: Thomasville Medical Assoc.. Device class: 2.

Clearance details

Applicant: Thomasville Medical Assoc.
Product code: Code HFX
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1992-12-28
Decision date: 1994-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

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K926531 — HYSTERECTOMY FORCEPS1994-02-25
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Adverse events under product code HFX

product code HFX

Other: 3
Total: 3

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.