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

OCS-2 COLPOSCOPE

K Number: K852980 · Decision Oct 23, 1985
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
55
Applicant Total
142
Review Days
100

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Basic Information

Device Name
OCS-2 COLPOSCOPE
K Number
K852980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1630
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
July 15, 1985
Decision Date
October 23, 1985
Product Code
HEX
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HEX Colposcope (And Colpomicroscope)

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Other Clearances by Olympus Corp.

K Number Device Name
K915402 EW-10 AND EW-20
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K942338 OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES
K931763 HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS
K934835 FLOVAL
K931764 HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES
K915857 FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE
K931994 RESECTOSCOPE SHEATH
K933992 OLYMPUS SCLEROTHERAPY BALLOON
K934361 OLYMPUS CREATININE REAGENT
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