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

VITALMAX 4100

K Number: K953795 · Decision Jul 1, 1996
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
16
Applicant Total
18
Review Days
322

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Basic Information

Device Name
VITALMAX 4100
K Number
K953795
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1620
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pace Tech, Inc.
Date Received
August 14, 1995
Decision Date
July 1, 1996
Product Code
CBS
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBS Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)

Similar 510(k) Clearances

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

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Other Clearances by Pace Tech, Inc.

K Number Device Name
K951226 VITALMAX 4000/MINIPACK 3100/3000
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. →