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

FETAL-TEK CONTROL (IMMATURE/BORDERLINE)

K Number: K820772 · Decision May 12, 1982
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
280
Review Days
50

Basic Information

Device Name
FETAL-TEK CONTROL (IMMATURE/BORDERLINE)
K Number
K820772
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
HELENA LABORATORIES
Date Received
March 23, 1982
Decision Date
May 12, 1982
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

View all

Other Clearances by HELENA LABORATORIES

K Number Device Name
K131479 V8 SP NORMAL CONTROL, ABNORMAL CONTROL
K100103 SPECIALTY ASSAYED CONTROL-2
K061991 PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACA
K061069 SPIFE IFE-15 PENTAVALENT, MODEL 3456, SPIFE IFE-9 PENTAVALENT KIT, MODEL 3457, SPIFT IFE-6 PENTAVALENT KIT, MODEL 3458
K061014 ACTALYKE QC KIT, MODELS AQC-HP AND AQC-LP
K050053 HEMORAM/AGGRAM ANALYZER
K024162 SPIFE 3000 TITAN GEL IGG IEF KIT, MODEL 3389
K023761 PLATELETWORKS, MODELS PW-A, PW-C
K022757 SPIFE CK KIT, MODEL 3332, 3333
K022455 SPIFE LD-12 KIT, MODEL 3338
Search all 280 clearances from HELENA LABORATORIES →