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

MICROLINE CAT #100

K Number: K880943 · Decision May 26, 1988
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
12
Review Days
80

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Basic Information

Device Name
MICROLINE CAT #100
K Number
K880943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Microline Pentax, Inc.
Date Received
March 7, 1988
Decision Date
May 26, 1988
Product Code
HQE
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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K Number Device Name
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K982984 ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS
K981389 DISPOSABLE RE-NEW FORCEPS
K981188 ELECTROSURGICAL CAUTERY PROBES
K980758 3 MM SELEC-TIP LAPAROSCOPIC SCISSORS
K974066 RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS
K970826 SELECTA-TIP LAPAROSCOPIC SCISSORS
K962119 RE-NEW LAPAROSCOPIC INSTRUMENTS
K932648 QUICK SWITCH LAPAROSCOPIC INSTRUMENTS
K897093 INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.
Search all 12 clearances from Microline Pentax, Inc. →