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

VITALMAX 4000/MINIPACK 3100/3000

K Number: K951226 · Decision Nov 21, 1996
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
76
Applicant Total
18
Review Days
612

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Basic Information

Device Name
VITALMAX 4000/MINIPACK 3100/3000
K Number
K951226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1110
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pace Tech, Inc.
Date Received
March 20, 1995
Decision Date
November 21, 1996
Product Code
DSK
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
DSK Computer, Blood-Pressure

Similar 510(k) Clearances

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

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Other Clearances by Pace Tech, Inc.

K Number Device Name
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
K913263 VITALMAX 830 SERIES
Search all 18 clearances from Pace Tech, Inc. →