Atlas FDA

FERRITIRON KIT CAT. #RP-1100

FDA 510(k) clearance K800710 · decided 1980-05-14

Clearance details

K-number
K800710
Device name
FERRITIRON KIT CAT. #RP-1100
Applicant
Ria Products, Inc.
Decision
Substantially Equivalent
Date received
1980-03-31
Decision date
1980-05-14
Days to decision
44 days
Clearance type
Traditional
Product code
JQG
Device class
1
Regulation number
862.1415
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
COMBO-FER IRON DIAGNOSTIC (K811954)Immuno Assay Corp.1981-07-27
FERRO-QUANT TM FE 59 TEST KIT (K800868)Mallinckrodt Critical Care1980-04-29
SPINSEP-FE59 (K790133)Nuclear Diagnostics, Inc.1979-03-02
TOTAL IRON BINDING CAPACITY (K780412)Diagnostic Corp. of America1978-05-26

Recalls involving this device

No recalls on record reference this clearance.