SERRATED GRASPING FORCEPS, RIGHT— 510(k) K873512

Name: FDA 510(k) clearance K873512
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Arthropedics, Inc.

FDA 510(k) clearance K873512 for SERRATED GRASPING FORCEPS, RIGHT, Substantially Equivalent on 1987-11-02. Applicant: Arthropedics, Inc.. Device class: 1.

Clearance details

Applicant: Arthropedics, Inc.
Product code: Code HTD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-08-31
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallington, NJ, US

Download summary PDF View on FDA.gov ↗

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K913964 — MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS1991-10-23

More clearances from Arthropedics, Inc.

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K873619 — ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)1988-01-14
K873653 — MONOPOLAR CAUTERY BLADE TIP #TM-17011987-12-15
K873654 — MONOPOLAR CAUTERY CONICAL TIP #TM-17021987-12-15
K873655 — MONOPOLAR CAUTERY RETROGADE TIP #TM-17031987-12-15
K873387 — VIDEO ARTHROSCOPE, 1.7MM X 55 MM1987-11-25

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.