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

CHARLES PNEUMATIC INTRAOCULAR SCISSORS

K Number: K801850 · Decision Sep 16, 1980
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
7
Review Days
43

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Basic Information

Device Name
CHARLES PNEUMATIC INTRAOCULAR SCISSORS
K Number
K801850
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cooper Medical Devices Corp.
Date Received
August 4, 1980
Decision Date
September 16, 1980
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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K801312 THE PROTECTORS
K800833 VABRA ASPIRATOR
K791898 OCUTOME MODEL 8000