FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

JAKOBI SURG. INSTRUMENTS #2 70/71

K Number: K834193 · Decision Feb 10, 1984
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
52
Review Days
81

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Basic Information

Device Name
JAKOBI SURG. INSTRUMENTS #2 70/71
K Number
K834193
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Imm Enterprises , Ltd.
Date Received
November 21, 1983
Decision Date
February 10, 1984
Product Code
FRG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRG Wrap, Sterilization

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Other Clearances by Imm Enterprises , Ltd.

K Number Device Name
K840311 CAT. 7-EAR, NOSE & THROAT DEVICES
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K841386 KOLLMANN URETHRAL DILATOR
K840304 CATEGORY 17-MICROBIOLOGY DEVICES
K840318 CAT. 14-CLINICAL TOXIOLOGY DEVICES
K840305 CATEGORY 1 CIRCULATORY SYSTEM DEVICE
K840312 CAT. 8 DENTAL DEVICES
K834171 OP-CON SURG. INSTRUMENT #3
K834191 JAKOBI SURGICAL INSTRUMENTS #3 17/18/19
K834192 JAKOBI SURG. INSTRUMENTS #3 21/22/24
Search all 52 clearances from Imm Enterprises , Ltd. →