FDA 510(k) Substantially Equivalent 🇺🇸 United States

CILCO ASCAN

K Number: K827371 · Decision Jul 9, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
12
Review Days
102

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Basic Information

Device Name
CILCO ASCAN
K Number
K827371
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Cilco, Inc.
Date Received
March 29, 1982
Decision Date
July 9, 1982
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

Other Clearances by Cilco, Inc.

K Number Device Name
K861334 CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE
K854969 CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)
K844249 K-SOL
K843319 CILCO I/A SURGICAL PACK
K843992 CILCOR OPHTHALMIC INSTRUMENTS
K843447 CILCO DIAMOND KNIFE
K841099 OCTOPUS 500/500E
K840475 CYSTOTOME, 140-S
K832405 OPTHALMIC ENDOSCOPE
K820933 CILCO I/A HANDPIECE
Search all 12 clearances from Cilco, Inc. →