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

PREDICTOR

K Number: K780240 · Decision Feb 27, 1978
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
223
Applicant Total
41
Review Days
14

Basic Information

Device Name
PREDICTOR
K Number
K780240
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
ORGANON, INC.
Date Received
February 13, 1978
Decision Date
February 27, 1978
Product Code
LCX
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
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

Similar 510(k) Clearances

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

View all

Other Clearances by ORGANON, INC.

K Number Device Name
K950861 RECONSTITUTION ACCESSOREIS
K853388 MONOSTICON UNI-DOT
K842314 DUOCLON COLOR-CEPT
K841525 OREIA II B-HCG PREGNANCY TEST KIT
K841602 ACCURATE BETA 30 PREGNANCY TEST KIT
K840650 B-NEOCEPT 30
K832801 OREIA II B-HCG, ENZYME INNUNOASSAY
K831339 NEO-PREGNOSTICON DUOCLON TUBE TEST
K831109 DUOCLON SLIDE TEST
K823682 BETA FFIRM TEST
Search all 41 clearances from ORGANON, INC. →