JAKOBI SURG. INSTRUMENTS #1 19/10/26— 510(k) K834194

Name: FDA 510(k) clearance K834194
Creator: U.S. Food and Drug Administration
Published: 1984-01-27

Substantially Equivalent

Imm Enterprises , Ltd.

FDA 510(k) clearance K834194 for JAKOBI SURG. INSTRUMENTS #1 19/10/26, Substantially Equivalent on 1984-01-27. Applicant: Imm Enterprises , Ltd.. Device class: 1.

Clearance details

Applicant: Imm Enterprises , Ltd.
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1983-11-21
Decision date: 1984-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GES

view all

K032242 — PERSONNA PLUS SAFETY SCALPEL SYSTEM2003-09-23
K932998 — EASY-ON1993-08-18
K923170 — LOS ALAMOS RETRACTABLE KNIFE1993-02-18
K915119 — SCALPEL BLADE REMOVER (BLADEGARD)1992-05-05
K911913 — PRECISION GLIDE - ENHANCED SURGICAL BLADE1991-05-13

More clearances from Imm Enterprises , Ltd.

view all

K840311 — CAT. 7-EAR, NOSE & THROAT DEVICES1984-05-09
K841386 — KOLLMANN URETHRAL DILATOR1984-05-09
K841387 — WESTON RECTAL SNARE1984-05-09
K840304 — CATEGORY 17-MICROBIOLOGY DEVICES1984-05-01
K840305 — CATEGORY 1 CIRCULATORY SYSTEM DEVICE1984-04-23

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