Atlas FDA

AHBD

FDA 510(k) clearance K822739 · decided 1982-10-18

Clearance details

K-number
K822739
Device name
AHBD
Applicant
Gilford Diagnostics
Decision
Substantially Equivalent
Date received
1982-09-09
Decision date
1982-10-18
Days to decision
39 days
Clearance type
Traditional
Product code
JMK
Device class
1
Regulation number
862.1380
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, 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
MTM BIOSCANNER K TEST STRIPS, CAT # BSA610 (K983860)Polymer Technology Systems, Inc.1999-12-27
MTM BIOSCANNER K TEST STRIPS (K981865)Polymer Technology Systems, Inc.1999-02-26
KETOREX C SANWA (K953452)Ihara Medics U.S., Inc.1996-05-02
SERUM @-HYDROXYBUTYRATE DEHYDROGENASE (HBDH) (K941427)Teco Diagnostics1995-03-13
HBDH (OPTIMIZED) REAGENT (K862319)Sigma Chemical Co.1986-07-07
RAICHEM X-HBDH REAGENT (K843774)Reagents Applications, Inc.1984-10-31
ULTRAZYME PLUS HBD (K821877)Harleco Diagnostics1982-07-14
HBDH ENZYME KINETIC REAGENT SET (K781720)Medical Analysis Systems, Inc.1978-11-03
ULTRAZYME PLUS HBD (K780104)Harleco1978-02-13
HBDH REAGENT SET (K780073)Medical Analysis Systems, Inc.1978-02-13
HYDORRYBUTYRATE DEHYDROGENASE (K780042)Beckman Instruments, Inc.1978-02-01
GEMSAEC APPLI. FOR ULTRAZYME PLUS ALP* (K772033)Harleco1977-11-17

Recalls involving this device

No recalls on record reference this clearance.