FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CAT. 4-OBSTETRICS GYNECOLOGY DEV'S

K Number: K840308 · Decision Mar 5, 1984
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
14
Applicant Total
52
Review Days
41

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Basic Information

Device Name
CAT. 4-OBSTETRICS GYNECOLOGY DEV'S
K Number
K840308
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4520
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Imm Enterprises , Ltd.
Date Received
January 24, 1984
Decision Date
March 5, 1984
Product Code
KOH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
KOH Instrument, Manual, General Obstetric-Gynecologic

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Other Clearances by Imm Enterprises , Ltd.

K Number Device Name
K840311 CAT. 7-EAR, NOSE & THROAT DEVICES
K841387 WESTON RECTAL SNARE
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
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