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

INTRAUTERINE DEVICE REMOVER

K Number: K842295 · Decision Oct 12, 1984
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
5
Applicant Total
41
Review Days
123

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
INTRAUTERINE DEVICE REMOVER
K Number
K842295
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Premier Dental Products Co.
Date Received
June 11, 1984
Decision Date
October 12, 1984
Product Code
HHF
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
HHF Remover, Intrauterine Device, Contraceptive, Hook-Type

Similar 510(k) Clearances

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

View all

Other Clearances by Premier Dental Products Co.

K Number Device Name
K141839 PREMIER ETCH
K132526 KNIT-PAK+
K131212 PREMIER CERAMIC PRIMER
K083695 TRAXODENT
K062683 ENAMEL PRO VARNISH
K062166 ENAMEL PRO
K061997 PREMIER SELF-ETCHING ENAMEL SEALANT
K061998 PREMIER SELF-ETCHING BOND ENHANCER
K051866 PREMIER TEMPORARY CEMENT
K042215 RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT
Search all 41 clearances from Premier Dental Products Co. →