FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ENZLIPASE, ENZYMATIC LIPASE KIT

K Number: K862312 · Decision Sep 26, 1986
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
19
Applicant Total
22
Review Days
100

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Basic Information

Device Name
ENZLIPASE, ENZYMATIC LIPASE KIT
K Number
K862312
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1465
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Nuclear Diagnostics, Inc.
Date Received
June 18, 1986
Decision Date
September 26, 1986
Product Code
CHI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CHI Lipase-Esterase, Enzymatic, Photometric, Lipase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CHI), ordered by most recent decision date.

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Other Clearances by Nuclear Diagnostics, Inc.

K Number Device Name
K923917 ELIPASE HUMAN PANCREATIC LIPASE ENZYMEIMMUNOASSAY
K932406 NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT
K872177 TIPSEP-CORTISOL RIA DIAGNOSTIC KIT
K860472 NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESS
K861735 TIPSEP-TBG ASSAY
K852291 TIPSEP DIGOXIN RIA
K833713 SERUM THYROTROPIN ASSAY KIT, TIPSEP-
K823860 NUCLIPASE (I125) PANCREATIC LIPASE
K811558 TSH-P.E.G.
K810906 TRI-LEVEL NDI CONTROL
Search all 22 clearances from Nuclear Diagnostics, Inc. →