FORCEP— 510(k) K812205

Substantially Equivalent

Reznik Instruments

FDA 510(k) clearance K812205 for FORCEP, Substantially Equivalent on 1981-10-26. Applicant: Reznik Instruments. Device class: 1.

Clearance details

Applicant: Reznik Instruments
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-08-04
Decision date: 1981-10-26
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 Reznik Instruments

K812201 — PHOTOGRAPHIC EQUIPMENT1981-10-19
K812199 — TROCAR & TROCAR SLEEVES1981-10-13
K812203 — ELECTROSURGICAL UNIT1981-10-13
K812204 — UTERINE MANIPULATORS1981-10-13
K812206 — LAPAROSCOPE1981-10-13

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