FORCEP, DISP., A CLAMP— 510(k) K771097

Name: FDA 510(k) clearance K771097
Creator: U.S. Food and Drug Administration
Published: 1977-07-14

Substantially Equivalent

Dravon Medical, Inc.

FDA 510(k) clearance K771097 for FORCEP, DISP., A CLAMP, Substantially Equivalent on 1977-07-14. Applicant: Dravon Medical, Inc.. Device class: 1.

Clearance details

Applicant: Dravon Medical, Inc.
Product code: Code HTD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-06-20
Decision date: 1977-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HTD

view all

K051281 — THE NEEDLE CATCHER2005-09-08
K974593 — SEMKIN INSULATED BIPOLAR FORCEP1998-06-24
K974594 — SEMKIN BIPOLAR FORCEP1998-06-24
K974595 — CUSHING BAYONET, INSULATED BIPOLAR FORCEP1998-06-24
K913964 — MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS1991-10-23

More clearances from Dravon Medical, Inc.

view all

K873455 — S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS1987-09-14
K860770 — AM-100 I/A AMPAC1986-04-21
K832739 — STEDIFLO INFUSION SET1983-12-22
K831842 — DRAVON T CLAMP1983-09-26
K812771 — PERITONEAL DIALYSIS DRAINAGE1981-10-19

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.