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

HM-0690 COLPOSCOPE

K Number: K932896 · Decision Mar 23, 1994
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
55
Applicant Total
10
Review Days
282

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Basic Information

Device Name
HM-0690 COLPOSCOPE
K Number
K932896
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1630
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hill-Med, Inc.
Date Received
June 14, 1993
Decision Date
March 23, 1994
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)

Similar 510(k) Clearances

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Other Clearances by Hill-Med, Inc.

K Number Device Name
K993991 HM-930 ELECTROSURGICAL UNIT
K981781 ELECTROSURGICAL UNIT
K961473 HM-88011 SOLID STATE ELECTR SURGICAL UNIT
K951718 HM-SPIRO
K940140 HM-CRYO
K932782 HM-0660
K932817 HM-880 I
K932818 HM-880
K932720 HM-0970