Atlas FDA

OSM3 HEMOXIMETER

FDA 510(k) clearance K853990 · decided 1985-12-30

Clearance details

K-number
K853990
Device name
OSM3 HEMOXIMETER
Applicant
Radiometer America, Inc.
Decision
Substantially Equivalent
Date received
1985-09-27
Decision date
1985-12-30
Days to decision
94 days
Clearance type
Traditional
Product code
JKS
Device class
1
Regulation number
862.3220
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Westlake, OH, 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
AVOXIMETER 4000 (K951485)A-Vox Systems, Inc.1995-11-06
CO-OXIMETER SOLUTIONS (K863825)D.R.G. Scientific Industries1986-11-24
IL 482 CO-OXIMETER (K862253)Instrumentation Laboratory CO1986-07-29
TEE ADAPTER 9890-FLUSH WINDING 282 (K833693)Shaban Mfg. Co.1983-12-30
BILE SALTS MIXTURE (K833211)Acumedia Manufacturers, Inc.1983-10-27
CONTROL 282 (K832066)Bio-Nustics, Inc.1983-09-29
HEMOGLOBIN CHECK SOLUTIONS, S2100 OSM-2 (K780652)The London Co.1978-07-27

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
RADIOMETER TCM-10 TRANSCUTANEOUS CARBON DIOXIDE MO (P800043/S004)Radiometer America, Inc.1986-02-21
RADIOMETER TCM-10 TRANSCUTANEOUS CARBON DIOXIDE MO (P800043/S003)Radiometer America, Inc.1985-02-22
RADIOMETER TCM-10 TRANSCUTANEOUS CARBON DIOXIDE MO (P800043/S002)Radiometer America, Inc.1984-03-01
RADIOMETER TCM-10 TRANSCUTANEOUS CARBON DIOXIDE MO (P800043/S001)Radiometer America, Inc.1981-09-21