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

FIRST RESPONSE 10 MINUTE OVULATION PREDICTOR TEST

K Number: K883530 · Decision Dec 19, 1988
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
70
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
FIRST RESPONSE 10 MINUTE OVULATION PREDICTOR TEST
K Number
K883530
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tambrands, Inc.
Date Received
August 18, 1988
Decision Date
December 19, 1988
Product Code
CEP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CEP Radioimmunoassay, Luteinizing Hormone

Similar 510(k) Clearances

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

View all

Other Clearances by Tambrands, Inc.

K Number Device Name
K962476 UNSCENTED MENSTRUAL TAMPON, PLASTIC APPLICATOR
K960341 TAMPAX TAMPON WITH ADDITIVE JUNIOR,REGULAR,SUPER, AND SUPER PLUS
K952344 SATIN TOUCH DEODORANT TAMPON JUNIOR, REGULAR, SUPER, SUPER PLUS
K944834 UNSCENTED MENSTRUAL TAMPONS
K923932 TAMPAX TAMPONS, SUPER ABSORBENCY
K924303 TAMPAX TAMPON, REGULAR ABSORBENCY
K896989 TAMPAX TAMPON
K896115 TAMPON, PETAL SOFT PLASTIC APPLI., DEODORANT SUPER
K896112 TAMPAX TAMPON, FLUSHABLE APPLICATOR, SUPER PLUS
K896113 TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS
Search all 70 clearances from Tambrands, Inc. →