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

VITA-STAT MODEL 900-D

K Number: K792193 · Decision Nov 20, 1979
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
5
Review Days
19

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VITA-STAT MODEL 900-D
K Number
K792193
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Vita-Stat Medical Services, Inc.
Date Received
November 1, 1979
Decision Date
November 20, 1979
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXN), ordered by most recent decision date.

View all

Other Clearances by Vita-Stat Medical Services, Inc.

K Number Device Name
K830713 LS-1 PORTABLE BLOOD PRESSURE COMPUTER
K830368 AMBULATORY BLOOD PRESSURE MONITOR
K792194 VITA-STAT MODEL 900-S
K792192 VITA-STAT MODEL 900A