Atlas FDA

ADP REAGENT

FDA 510(k) clearance K910800 · decided 1991-05-20

Clearance details

K-number
K910800
Device name
ADP REAGENT
Applicant
Helena Laboratories
Decision
Substantially Equivalent
Date received
1991-02-25
Decision date
1991-05-20
Days to decision
84 days
Clearance type
Traditional
Product code
GHR
Device class
2
Regulation number
864.5700
Medical specialty
Hematology
Advisory committee
Hematology
Location
Beaumont, TX, 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
PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACA (K061991)Helena Laboratories2007-02-23
ADP REAGENT, MODIFIED (K952252)Helena Laboratories1995-09-08
PLATELET AGGREGATION REAGENTS (K922800)Chrono-Log Corp.1992-08-26
COLLAGEN REAGENT CAT. NO. 5368 (K910706)Helena Laboratories1991-05-20
EPINEPHRINE REAGENT, CAT. NO. 5367 (K910680)Helena Laboratories1991-05-20
PLATELET AGGREGATION REAGENTS (K910286)Medical Diagnostic Technologies, Inc.1991-03-19
RISTOCETIN (K900792)Medical Diagnostic Technologies, Inc.1990-03-27
PLATELET AGGREGATION REAGENT SET (K832428)Helena Laboratories1983-10-20
PLATELET AGGREGOMETERS (K820422)Chrono-Log Corp.1982-03-16
KIT, PLATELET AGGREGATION REAGENT (#390) (K760198)Chrono-Log Corp.1976-07-19

Recalls involving this device

No recalls on record reference this clearance.