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

VITAL SYSTEM

K Number: K880351 · Decision Mar 22, 1988
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
18
Review Days
56

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
VITAL SYSTEM
K Number
K880351
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pace Tech, Inc.
Date Received
January 26, 1988
Decision Date
March 22, 1988
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 Pace Tech, Inc.

K Number Device Name
K951226 VITALMAX 4000/MINIPACK 3100/3000
K953795 VITALMAX 4100
K944541 HANDYPACK 911SC
K945385 VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
K925701 MINIPACK 911-STC
K934385 MINIPACK 3100/3000 MODIFICATION
K933624 VITALMAX 4000
K930559 VITALMAX 800-C
K912835 MINI-PACK 911 SERIES
K912880 VITALMAX 510/520
Search all 18 clearances from Pace Tech, Inc. →