Atlas FDA

SR1 DHEA-S ENZYME IMMUNOASSAY

FDA 510(k) clearance K942051 · decided 1994-07-13

Clearance details

K-number
K942051
Device name
SR1 DHEA-S ENZYME IMMUNOASSAY
Applicant
Serono Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1994-04-28
Decision date
1994-07-13
Days to decision
76 days
Clearance type
Traditional
Product code
JKC
Device class
1
Regulation number
862.1245
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Allentown, PA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Serono Diagnostics

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
ACCESS DHEA-S REAGENT ASSAY (K040181)Beckman Coulter, Inc.2004-03-24
ELECSYS DHEA-S (K003174)Roche Diagnostics Corp.2001-01-17
DHEA-S (K973897)Kmi Diagnostics, Inc.1997-11-13
DSL DHEA-S-7 (K962895)Diagnostic Systems Laboratories, Inc.1996-09-10
DSL AACTIVE DHEA EIA KIT (K955114)Diagnostic Systems Laboratories, Inc.1996-02-23
NICHOLS INSTITUTE DIAGNOSTICS DHEA-S CHEMILUMINESCENCE IMMUNOASSAY (K950524)Nichols Institute1995-05-15
ACTIVE DEHYDROEPIANDROSTERONE (DHEA)(DSL 9000) (K935014)Diagnostic Systems Laboratories, Inc.1994-05-09
IMMULITE DHEA-S04 (K935806)Diagnostic Products Corp.1994-04-26
SYNELISA DHEA-SULFATE (K935469)Elias U.S.A., Inc.1994-03-22
CHEMILUMINESCENCE DHEA-S IMMUNOASSAY (K931601)Nichols Institute1993-07-27
DSL ANDROSTANEDIOL GLUCURONIDE (DSL #6000) (K903616)Diagnostic Systems Laboratories, Inc.1990-09-10
DSL 7900 ACTIVE DHEA-S (DSL #7900) (K891478)Diagnostic Systems Laboratories, Inc.1989-04-26

Recalls involving this device

No recalls on record reference this clearance.