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

GENT-L-SPEC DISPOS. VAGINAL SPECULUM

K Number: K830725 · Decision Apr 27, 1983
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
71
Applicant Total
13
Review Days
50

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Basic Information

Device Name
GENT-L-SPEC DISPOS. VAGINAL SPECULUM
K Number
K830725
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Geneva Laboratories, Inc.
Date Received
March 8, 1983
Decision Date
April 27, 1983
Product Code
HIB
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
HIB Speculum, Vaginal, Nonmetal

Similar 510(k) Clearances

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Other Clearances by Geneva Laboratories, Inc.

K Number Device Name
K881217 GENT-L-KARE STERILE URINARY LEG BAG
K881213 GENT-L-KARE STERILE URINARY DRAINAGE BAG CENTER
K881218 GENT-L-KARE CLEANSING ENEMA SET
K881216 GENT-L-KARE VAGINAL IRRIGATION SET
K861308 ACCUPAC CUSTOM PACK KERLIX SQUARES
K861219 ACCUPAC CUSTOM SKIN SCRUB KIT
K853265 ACCUPAC CUSTOM OPERATING ROOM PROCEDURE-DK876543
K843206 COOK COUNTY HOSPITAL DRESSING CHANGE SET
K844255 GENT-L-KARE STERILE I.V. START KIT
K843090 UNIVERSITY OF CHICAGO VASCULAR ANGIOGRAM
Search all 13 clearances from Geneva Laboratories, Inc. →