FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GENT-L-KARE VAGINAL IRRIGATION SET

K Number: K881216 · Decision Jun 7, 1988
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
11
Applicant Total
13
Review Days
77

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Basic Information

Device Name
GENT-L-KARE VAGINAL IRRIGATION SET
K Number
K881216
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.5900
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Geneva Laboratories, Inc.
Date Received
March 22, 1988
Decision Date
June 7, 1988
Product Code
HED
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
HED Douche Apparatus, Vaginal, Therapeutic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HED), ordered by most recent decision date.

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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
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
K830725 GENT-L-SPEC DISPOS. VAGINAL SPECULUM
Search all 13 clearances from Geneva Laboratories, Inc. →