Atlas FDA

LIPASE REAGENT SET

FDA 510(k) clearance K790796 · decided 1979-07-17

Clearance details

K-number
K790796
Device name
LIPASE REAGENT SET
Applicant
Alta Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1979-04-24
Decision date
1979-07-17
Days to decision
84 days
Clearance type
Traditional
Product code
CET
Device class
1
Regulation number
862.1465
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
LIPASE REAGENT SET (COLIPASE METHOD) (K970124)Teco Diagnostics1997-03-06
LIPASE REAGENT SYSTEM (K940457)Medical Diagnostic Technologies, Inc.1994-06-02
LIPASE REAGENT SET (K915706)Tech Intl. Co.1992-02-18
MODIFIED LABELING FOR ACA LIPASE ANALYTICAL TEST (K901858)E.I. Dupont DE Nemours & Co., Inc.1990-06-12
DELTATEST (R) LIPASE II (K893718)Electro-Nucleonics, Inc.1989-09-28
LIPASE SR LIQUID STABLE REAGENT SET (K885078)Medical Analysis Systems, Inc.1989-03-13
BECKMAN EPSILON(TM) LIPASE TEST KIT (K864438)Beckman Instruments, Inc.1987-03-12
PARAMAX LIPASE REAGENT (K862440)American Dade1986-08-04
ENZYGNOST LIPASE TEST (K844240)Behring Diagnostics, Inc.1985-02-12
NUCLIPASE (I125) PANCREATIC LIPASE (K823860)Nuclear Diagnostics, Inc.1983-04-18
LIPASE (K812794)Pointe Scientific, Inc.,1981-10-20
LIPASE TEST KIT (K792289)Mallinckrodt Critical Care1979-12-18

Recalls involving this device

No recalls on record reference this clearance.