Atlas FDA

PRECISION GAS MIXER

FDA 510(k) clearance K781417 · decided 1978-09-20

Clearance details

K-number
K781417
Device name
PRECISION GAS MIXER
Applicant
Medicor USA , Ltd.
Decision
Substantially Equivalent
Date received
1978-08-16
Decision date
1978-09-20
Days to decision
35 days
Clearance type
Traditional
Product code
LCH
Device class
1
Regulation number
862.1660
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
RNA MEDICAL TONOMETER (K922386)Bionostics, Inc.1992-06-26
CLINICAL BLOOD GAS MIXTURES (K904163)Norco, Inc.1990-11-01
BLOOD GAS CALIBRATION STANDARD (K900819)Cryogenic Rare Gas Laboratories, Inc.1990-04-25
AMR RESEARCH TONOMETER (K862958)Associated Medical Representatives1986-11-24
LINEAR CLOUD TONOMETER (K841089)Linear Tonometers, Inc.1984-05-22
HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZER (K802379)American Instrument Co.1980-10-31
CORNING 184 BLOOD GAS TONOMETER (K801599)Corning Medical & Scientific1980-08-20
EBS 775 TONOMETER (K781386)Equilibrated Bio Systems, Inc.1978-09-14

Recalls involving this device

No recalls on record reference this clearance.