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

CATEGORY 6 OPTHALMIC DEVICES

K Number: K840310 · Decision Mar 16, 1984
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
2
Applicant Total
52
Review Days
52

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Basic Information

Device Name
CATEGORY 6 OPTHALMIC DEVICES
K Number
K840310
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Imm Enterprises , Ltd.
Date Received
January 24, 1984
Decision Date
March 16, 1984
Product Code
HOB
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
HOB Clamp, Muscle, Ophthalmic

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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. →