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

BINOCULAR MAGNIFIER 2X

K Number: K830774 · Decision Apr 6, 1983
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
0
Applicant Total
21
Review Days
26

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Basic Information

Device Name
BINOCULAR MAGNIFIER 2X
K Number
K830774
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.5540
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Almore Intl., Inc.
Date Received
March 11, 1983
Decision Date
April 6, 1983
Product Code
HKC
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
HKC Spectacle Microscope, Low-Vision

Other Clearances by Almore Intl., Inc.

K Number Device Name
K862851 ALMORE FACE MASK
K854692 MONARCH II BLEACHING INSTRUMENT
K854696 OP II VISIBLE LIGHT CURING SYSTEM
K854690 DIAMONDS BURS-COMPOSIT FINISHING
K854691 DIAMOND BURS-HANDPIECE
K854700 EZ-ON TUBING CONDITIONER (LUBRICANT)
K854702 PLASTIC MOUNTING RINGS
K854701 RETRACT-A-CORD
K854697 TUBING HANDPIECE REPLACEMENT
K854699 TUBING SYRING
Search all 21 clearances from Almore Intl., Inc. →