Atlas FDA

HGB-CAL SET/MULTIPLE

FDA 510(k) clearance K893984 · decided 1989-08-15

Clearance details

K-number
K893984
Device name
HGB-CAL SET/MULTIPLE
Applicant
R&D Systems, Inc.
Decision
Substantially Equivalent
Date received
1989-06-05
Decision date
1989-08-15
Days to decision
71 days
Clearance type
Traditional
Product code
KRZ
Device class
2
Regulation number
864.8165
Medical specialty
Hematology
Advisory committee
Hematology
Location
Minneapolis, MN, 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
C.F.A.S. (CALIBRATOR FOR AUTOMATED SYSTEMS) HBA1C (K052101)Roche Diagnostics2005-08-26
CDS HEMATOLOGY CALIBRATOR (CDS CAL) (K041130)Clinical Diagnostic Solutions, Inc.2004-06-10
THB CAL STANDARD FOR IL CO-OXIMETERS/OXIMETERS (K962864)Alko Diagnostic Corp.1996-12-18
ALKO SLOPE THB SOLUTION FOR CORNING 280, 288 AND 2500 ANALYZERS (K951071)Alko Diagnostic Corp.1995-07-24
CELL-DYN CALIBRATOR (K902892)Unipath , Ltd.1990-09-10
RAICHEM TM HEMOGLOBIN CALIBRATOR (K896921)Reagents Applications, Inc.1990-01-25
MSI-CAL 16 (K883850)Medical Specialties, Inc.1988-11-22
MSI-CAL 7 (K883703)Medical Specialties, Inc.1988-11-22
MSI-CAL 8 (K883851)Medical Specialties, Inc.1988-11-22
HEMOCUE HEMOGLOBIN CALIBRATOR (K882600)React and Co.1988-07-18
REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 (K873832)In Vitro Diagnostics, Inc.1987-11-23
CYANMETHEMOGLOBIN STANDARD (K871283)U. S. Diagnostics, Inc.1987-04-15

Recalls involving this device

No recalls on record reference this clearance.