CANNULATED BIOPSY FORCEPS— 510(k) K926430

Name: FDA 510(k) clearance K926430
Creator: U.S. Food and Drug Administration
Published: 1993-03-26

Substantially Equivalent

Thomasville Medical Assoc.

FDA 510(k) clearance K926430 for CANNULATED BIOPSY FORCEPS, Substantially Equivalent on 1993-03-26. Applicant: Thomasville Medical Assoc.. Device class: 2.

Clearance details

Applicant: Thomasville Medical Assoc.
Product code: Code EOQ
Device class: Class 2
Regulation: 21 CFR 874.4680
Advisory panel: Ear, Nose, Throat
Date received: 1992-12-23
Decision date: 1993-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Thomasville Medical Assoc.

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K926429 — VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT1994-02-28
K926471 — MOGAN CIRCUMCISION CLAMP1994-02-25
K926484 — CORSON MYOMA GRASPING FORCEPS1994-02-25
K926527 — ROTO FIT BIOPSY FORCEPS1994-02-25
K926531 — HYSTERECTOMY FORCEPS1994-02-25

Adverse events under product code EOQ

product code EOQ

Death: 135
Injury: 2,863
Malfunction: 21,662
Total: 24,660

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.