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

BLOOD PRESSURE DEVICE, 400 SERIES

K Number: K781906 · Decision Nov 16, 1978
Classifications
1
FEI Numbers
420
Registration Numbers
420
Same Product Code
1186
Applicant Total
16
Review Days
3

Basic Information

Device Name
BLOOD PRESSURE DEVICE, 400 SERIES
K Number
K781906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
MED-TEK CORP.
Date Received
November 13, 1978
Decision Date
November 16, 1978
Product Code
DXN
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
DXN System, Measurement, Blood-Pressure, Non-Invasive

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K900428 ANESTHESIA BREATHING CIRCUITS
K901626 H.N. METAL BACKED ACETABULAR CUP, NONCEMENTED
K901594 H.N. TOTAL HIP PROSTHESIS
K901480 F-20 TOTAL HIP PROSTHESIS
K901273 L.M.S. SELF-DETACHABLE BROACH WITH STOP
K901272 ORION BLADE PLATE FOR TIBIAL OSTEOTOMY
K901240 ASTEL NON-METAL BACKED ACETABULAR CUP FOR CEMENTED
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