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

TSH IRMA KIT

K Number: K862249 · Decision Jun 27, 1986
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
240
Applicant Total
29
Review Days
15

Basic Information

Device Name
TSH IRMA KIT
K Number
K862249
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
PACIFIC BIOTECH, INC.
Date Received
June 12, 1986
Decision Date
June 27, 1986
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

Similar 510(k) Clearances

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

View all

Other Clearances by PACIFIC BIOTECH, INC.

K Number Device Name
K924461 STREP A NEGATIVE CONTROL
K902510 CARDS O.S. MONO
K896482 PERFECT(TM) ONE STEP EARLY PREGNANCY TEST KIT
K896221 CARDS O.S.(TM) STREP A
K895390 CARDS O.S. (TM) HCG-URINE
K891770 HCG IRMA II
K884616 FIRSTDAY EARLY PREGNANCY TESTING KIT II
K883742 MODIFIED TSH IRMA KIT
K884007 CARDS(TM) MONO
K882895 MODIFIED BETA QUIK STAT EIA KIT
Search all 29 clearances from PACIFIC BIOTECH, INC. →