Atlas FDA

SANTEST 1AP

FDA 510(k) clearance K862087 · decided 1986-12-03

Clearance details

K-number
K862087
Device name
SANTEST 1AP
Applicant
Scientific Sales Intl., Inc.
Decision
Substantially Equivalent
Date received
1986-06-02
Decision date
1986-12-03
Days to decision
184 days
Clearance type
Traditional
Product code
LKL
Device class
1
Regulation number
866.5420
Medical specialty
Immunology
Advisory committee
Immunology
Location
Kalamazoo, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
K-ASSAY ALPHA-1 AG (K993441)Kamiya Biomedical Co.1999-11-24
N-ASSAY TIA MULTI V-NL (K964299)Crestat Diagnostics, Inc.1997-07-14
IMMAGE IMMUNOCHEMISTRY SYSTEM ALPHA-1-ACID GLYCOPROTEIN (AAG) REAGENT (K964257)Beckman Instruments, Inc.1997-03-24
AL-ACID GLYCOPROTEIN RID KIT (K922417)The Binding Site, Ltd.1992-08-20
RAICHEM (TM) SPIA (TM) - ACID GLYCOPROTEIN REAGENT (K904175)Reagents Applications, Inc.1990-11-13
TECHNICON DPA-1 ANALYTE ALPHA 1 ACID GLYCOPROTEIN (K884217)Technicon Instruments Corp.1988-11-04
ALPHA-1-ACID GLYCOPROTEIN (OROSOMUCOID) (K873868)Unipath , Ltd.1987-10-20
IAP PLATE TEST (K861336)Scientific Sales Intl., Inc.1986-04-25
TAGO FIFFU-GEN, OROSOMUCOID (K841734)Tago, Inc.1984-06-01
TEST FOR HUMAN ALPHA ONE ACID GLYCO- (K831960)Kent Laboratories, Inc.1983-07-19

Recalls involving this device

No recalls on record reference this clearance.