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LYPOPROTEIN CHOLESTEROL TEST KIT

FDA 510(k) clearance K780173 · decided 1978-05-03

Clearance details

K-number
K780173
Device name
LYPOPROTEIN CHOLESTEROL TEST KIT
Applicant
Environmental Chemical Specialties
Decision
Substantially Equivalent
Date received
1978-02-02
Decision date
1978-05-03
Days to decision
90 days
Clearance type
Traditional
Product code
JHM
Device class
1
Regulation number
862.1475
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
PICCOLO HDL-CAPILLARY TEST SYSTEM (K120662)Abaxis, Inc.2012-04-24
DIMENSION VISTA HDLC FLEX REAGENT CARTRIDGE (K081300)Siemens Healthcare Diagnostics2008-07-02
DIMENSION AHDL FLEX REAGENT CARTRIDGE, MODEL: DF48B (K073072)Dade Behring, Inc.2008-02-21
DIMENSION AUTOMATED HDL CHOLESTEROL (AHDL) FLEX REAGENT CARTRIDGE (DF48A) CATALOG # DF48A (K032798)Dade Behring, Inc.2003-10-30
LDL CHOLESTEROL (AUTOMATED) (K022519)Jas Diagnostics, Inc.2002-09-30
DIMENSION AUTOMATED HIGH DENSITY LIPOPROTEIN CHOLESTEROL (ADHL) FLEX REAGENT CARTRIDGE (K983849)Dade Behring, Inc.1999-01-11
ROCHE COBAS READY HDL CHOLESTEROL REAGENT (K902935)Roche Diagnostic Systems, Inc.1990-09-27
HDL PRECIPITANT REAGENT SET (K841056)Medical Specialties, Inc.1984-05-01

Recalls involving this device

No recalls on record reference this clearance.