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

STERILE DISPOSABLE ENDOCULAR PROBE

K Number: K884456 · Decision Dec 9, 1988
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
11
Review Days
46

Basic Information

Device Name
STERILE DISPOSABLE ENDOCULAR PROBE
K Number
K884456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
BIOPHYSIC MEDICAL, INC.
Date Received
October 24, 1988
Decision Date
December 9, 1988
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEX Powered Laser Surgical Instrument

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K884595 OPHTHASCAN MINI-B
K883719 INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM
K881494 FOUR MODIFICATIONS TO OPHTHALAS ARGON/DYE LASER
K881459 NANOLAS ND:YAG OPHTHALMIC LASER
K873460 OPHTHALAS DYE OPHTHALMIC LASER
K853116 PAXIAL
K844686 OPHTHASCAN B
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