BACKHAUS CLAMP, 5 1/4— 510(k) K821293

Name: FDA 510(k) clearance K821293
Creator: U.S. Food and Drug Administration
Published: 1982-05-28

Substantially Equivalent

Conphar, Inc.

FDA 510(k) clearance K821293 for BACKHAUS CLAMP, 5 1/4, Substantially Equivalent on 1982-05-28. Applicant: Conphar, Inc.. Device class: 1.

Clearance details

Applicant: Conphar, Inc.
Product code: Code HTD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1982-05-04
Decision date: 1982-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Conphar, Inc.

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K821825 — CONPHAR SILICONE FEEDING TUBE1982-08-10
K821289 — MAYO-HEGAR NEEDLE HOLDER1982-06-03
K821295 — OLSEN HEGAR NEEDLE HOLDERS1982-06-03
K821354 — CONPHAR MAYO HEGAR NEEDLE HOLDER1982-06-03
K821248 — ROCHESTER PEAN FORCEPS1982-05-28

Adverse events under product code HTD

product code HTD

Malfunction: 892
Total: 892

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.