Atlas FDA

IRIS URINE STAIN

FDA 510(k) clearance K821503 · decided 1982-06-03

Clearance details

K-number
K821503
Device name
IRIS URINE STAIN
Applicant
Intl. Remote Imaging Systems
Decision
Substantially Equivalent
Date received
1982-05-19
Decision date
1982-06-03
Days to decision
15 days
Clearance type
Traditional
Product code
ICF
Device class
1
Regulation number
864.1850
Medical specialty
Hematology
Advisory committee
Hematology
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
TISSUE GRAM STAIN (K864531)Sigma Diagnostics, Inc.1986-12-22
VON WILLEBRAND FACTOR ANTIGEN SCREEN (K842537)American Dade1984-10-01
GENTIAN VIOLET (K842730)E K Ind., Inc.1984-08-03
VOLU-SOL URINARY SEDIMENT STAIN (K792495)Volu Sol Medical Industries1979-12-18

Recalls involving this device

No recalls on record reference this clearance.