Atlas FDA

HEMOCARD CONTROL

FDA 510(k) clearance K910431 · decided 1991-03-11

Clearance details

K-number
K910431
Device name
HEMOCARD CONTROL
Applicant
Isolab, Inc.
Decision
Substantially Equivalent
Date received
1991-02-01
Decision date
1991-03-11
Days to decision
38 days
Clearance type
Traditional
Product code
JCM
Device class
2
Regulation number
864.7415
Medical specialty
Hematology
Advisory committee
Hematology
Location
Akron, OH, 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
EXTENDSURE HBFASC CONTROL (K053031)Cantebury Scientific , Ltd.2005-12-07
HEMOGLOBIN F & A2 CONTROL (BETA-THALASSAEMIA CONTROL) (K011389)Canterbury Health Laboratories2001-06-21
MODIFICATION TO ABUSCREEN ONLINE FOR PHENCYCLIDINE (K983704)Roche Diagnostic Systems, Inc.1999-02-10
QUIK-SEP QUANTITIVE HEMOGLOBIN S CONTROLS (K942222)Isolab, Inc.1995-01-20
AFSC HEMO CONTROL #5331, AA2 HEMO CONTROL #5328 (K933086)Helena Laboratories1994-10-31
HEMOCARD CONTROL HB-AA, AE, FAA, FAE (K931234)Isolab, Inc.1993-05-11
HEMOCARD(TM) CONTROL (K924173)Isolab, Inc.1992-12-01
SICKLE HEMOGLOBIN (HBA/S) CONTROL SET (K913427)Creative Laboratory Products, Inc.1991-11-19
LYPHOCHEK(R) HEMOGLOBIN A2 CONTROL (K911347)Bio-Rad1991-06-10
HELENA ABNORMAL HBA2 QUIK COLUMN CONTROL (K820787)Helena Laboratories1982-04-08
SICKLE-CHECK (K820037)Diagnostic Technology, Inc.1982-02-04

Recalls involving this device

No recalls on record reference this clearance.