Atlas FDA

SERUM IRON

FDA 510(k) clearance K771838 · decided 1977-11-03

Clearance details

K-number
K771838
Device name
SERUM IRON
Applicant
Gamma Enterprises, Inc.
Decision
Substantially Equivalent
Date received
1977-09-21
Decision date
1977-11-03
Days to decision
43 days
Clearance type
Traditional
Product code
JIY
Device class
1
Regulation number
862.1410
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
DIMENSION VISTA IRON FLEX REAGENT CARTRIDGE AND CALIBRATOR (K061793)Dade Behring, Inc.2006-08-07
DIMENSION IRON FLEX REAGENT CARTRIDGE (IRON-DF85) (K060264)Dade Behring, Inc.2006-03-08
SENTINEL IRON LIQUID (K051115)Sentinel Ch. Srl2005-08-25
VITALAB IRON REAGENT (K033983)Clinical Data, Inc.2004-05-21
ATAC IRON REAGENT, ATAC TIBC COLUMN KIT AND IRON CALIBRATOR (500 UG/DL) (K030528)Clinical Data2003-06-17
IRON-PC-SL ASSAY MODEL # 151-10, 151-26 (K020816)Diagnostic Chemicals , Ltd.2002-05-14
WIENER LAB.FER-COLOR AA, MODEL 5X 20 ML CAT.N 1492003 (K013097)Wiener Laboratories Saic2001-11-13
IRON (K981241)Abbott Laboratories1998-05-01
SERUM IRON-SL ASSAY, CATALOGUE NUMBERS 157-10, 157-30 (K973933)Diagnostic Chemicals , Ltd.1997-11-04
IL TEST IRON (K972363)Instrumentation Laboratory CO1997-08-15
IRON REAGENT (K964913)Derma Media Lab., Inc.1997-02-20
TOTAL IRON (NITRO-PAPS) REAGENT SET (K961588)Pointe Scientific, Inc.,1996-11-18

Recalls involving this device

No recalls on record reference this clearance.