FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALBP

K Number: K981457 · Decision May 27, 1998
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
17
Applicant Total
14
Review Days
34

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Basic Information

Device Name
ALBP
K Number
K981457
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Mfg., Inc.
Date Received
April 23, 1998
Decision Date
May 27, 1998
Product Code
CJW
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
CJW Bromcresol Purple Dye-Binding, Albumin

Similar 510(k) Clearances

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Other Clearances by Abbott Mfg., Inc.

K Number Device Name
K981232 CA
K981231 CO2
K965230 ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP
K971293 LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE
K953656 ABBOTT IMX PROLACTIN(MODIFICATION)
K953657 ABBOTT AXSYM PROLACTIN(MODIFICATION)
K944669 FLEXIFLO QUANTUM ENTERAL PUMP
K943691 IMX FOLATE
K943733 FLEXIFLO SIX ENTERAL NUTRITION PUMP
K941214 LIFESHIELD EXTENSION SET
Search all 14 clearances from Abbott Mfg., Inc. →