FORCEPS— 510(k) K771746

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K771746 for FORCEPS, Substantially Equivalent on 1977-09-26. Applicant: Depuy, Inc.. Device class: 1.

Clearance details

Applicant: Depuy, Inc.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-09-15
Decision date: 1977-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEN

K031828 — NATURALASE LP ND:YAG LASER2003-07-17
K953962 — FORCEPS1995-09-08
K932385 — SUTURE REMOVING FORCEPS1993-08-06
K904723 — FORCEPS1991-07-26
K911159 — PALPATION PROBE1991-03-29

More clearances from Depuy, Inc.

K043058 — PINNACLE CONSTRAINED ACETABULAR LINERS2005-03-14
K042664 — LPS UPPER EXTREMITY2004-12-08
K041085 — LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY2004-07-22
K033959 — LPS2004-07-01
K040544 — DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -0622004-05-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.