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

JAKOBI SURG. INSTRUMENTS #6 50

K Number: K834187 · Decision Mar 5, 1984
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
52
Review Days
105

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Basic Information

Device Name
JAKOBI SURG. INSTRUMENTS #6 50
K Number
K834187
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Imm Enterprises , Ltd.
Date Received
November 21, 1983
Decision Date
March 5, 1984
Product Code
HKY
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HKY Tonometer, Manual

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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
Search all 52 clearances from Imm Enterprises , Ltd. →