Atlas FDA

Albumin BCP2

FDA 510(k) clearance K203530 · decided 2022-03-18

Clearance details

K-number
K203530
Device name
Albumin BCP2
Applicant
Abbott Ireland Diagnostics Division
Decision
Substantially Equivalent
Date received
2020-12-02
Decision date
2022-03-18
Days to decision
471 days
Clearance type
Traditional
Product code
CJW
Device class
2
Regulation number
862.1035
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Longford, IE
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
Albumin BCP (K193001)SENTINEL CH. SpA2019-12-19
ADVIA CHEMISTRY ALBUMIN BCP REAGENT (ALBP), ADVIA CHEMISTRY ALBUMIN BCP CALIBRATOR (K132664)Siemens Healthcare Diagnostics, Inc.2013-10-16
ALBUMIN REAGENT (K021636)Intersect Systems, Inc.2002-07-17
RANDOX ALBUMIN (K000483)Randox Laboratories, Ltd.2000-03-31
ALBUMIN BCG, MODEL AL 103-01 (K990978)A.P. Total Care, Inc.1999-05-25
ALBP (K981814)Abbott Laboratories1998-07-22
ALBP (K981457)Abbott Mfg., Inc.1998-05-27
ABBOTT QUICKSTART ALBUMIN BCP (ALBP)#5A16 (K913025)Em Diagnostic Systems, Inc.1991-10-09
ALBUMIN REAGENT SET (K905776)Biochemical Trade, Inc.1991-02-26
ALBUMIN (BCP) (K863226)Sigma Diagnostics, Inc.1986-09-17
EMDS(TM) ALBUMIN TESTPACKS, #67652/95 (K863004)Em Diagnostic Systems, Inc.1986-09-16
VISION ALBUMIN (K862138)Abbott Laboratories1986-06-17

Recalls involving this device

No recalls on record reference this clearance.