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

HANDYPACK 911SC

K Number: K944541 · Decision Feb 22, 1995
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
301
Applicant Total
18
Review Days
160

Basic Information

Device Name
HANDYPACK 911SC
K Number
K944541
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
PACE TECH, INC.
Date Received
September 15, 1994
Decision Date
February 22, 1995
Product Code
CCK
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
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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Other Clearances by PACE TECH, INC.

K Number Device Name
K951226 VITALMAX 4000/MINIPACK 3100/3000
K953795 VITALMAX 4100
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. →