FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODEL P-380 PHYSIOLOGICAL PRESSURE TRAN.

K Number: K801138 · Decision Jul 14, 1980
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
147
Applicant Total
4
Review Days
63

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Basic Information

Device Name
MODEL P-380 PHYSIOLOGICAL PRESSURE TRAN.
K Number
K801138
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2850
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Gics Pharmaceuticals
Date Received
May 12, 1980
Decision Date
July 14, 1980
Product Code
DRS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DRS Transducer, Blood-Pressure, Extravascular

Similar 510(k) Clearances

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Other Clearances by Gics Pharmaceuticals

K Number Device Name
K802890 CPS-1000
K801136 D300 DOME
K800849 TMS 1000 TEMP. MONITOR & PROBES