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

FIBEO OPTICS ILLUM. SYSTEM

K Number: K771918 · Decision Oct 20, 1977
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
12
Applicant Total
25
Review Days
8

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Basic Information

Device Name
FIBEO OPTICS ILLUM. SYSTEM
K Number
K771918
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Propper Mfg. Co., Inc.
Date Received
October 12, 1977
Decision Date
October 20, 1977
Product Code
GCP
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
GCP Endoscope, Ac-Powered And Accessories

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K991618 BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR
K991276 PASS/FAIL CHALLENGE PACK
K973585 PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR
K972747 BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)
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