Atlas FDA

OPUS ETHANOL

FDA 510(k) clearance K972011 · decided 1997-07-22

Clearance details

K-number
K972011
Device name
OPUS ETHANOL
Applicant
Behring Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1997-05-30
Decision date
1997-07-22
Days to decision
53 days
Clearance type
Traditional
Product code
DIC
Device class
2
Regulation number
862.3040
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Westwood, MA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
OPUS(R) CEA TEST SYSTEM (P920021/S001)Behring Diagnostics, Inc.1996-02-23