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

IRRIGATION & ASPIRATION/VITRECTOMY DEVICE

K Number: K862188 · Decision Aug 21, 1986
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
148
Applicant Total
14
Review Days
73

Basic Information

Device Name
IRRIGATION & ASPIRATION/VITRECTOMY DEVICE
K Number
K862188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
COBURN OPTICAL IND., INC.
Date Received
June 9, 1986
Decision Date
August 21, 1986
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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Other Clearances by COBURN OPTICAL IND., INC.

K Number Device Name
K892348 MAGNILINK SYSTEM 201
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K892347 MAGNILINK SYSTEM 101
K892349 MAGNILINK SYSTEM 209
K892350 MAGNILINK SYSTEM 402/5
K853457 COBURN I/A SYSTEM
K821737 DISP. MICROSURGICAL KNIVES
K812441 DI-CROWN
K803159 AUTOMATED PERIMETERS
K801659 BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPE
Search all 14 clearances from COBURN OPTICAL IND., INC. →