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

PEGASUS PROACTIVE WHEELCHAIR CUSHION

K Number: K930742 · Decision Mar 31, 1994
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
4
Review Days
412

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Basic Information

Device Name
PEGASUS PROACTIVE WHEELCHAIR CUSHION
K Number
K930742
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent for Some Indications
Applicant
Pegasus Airwave, Inc.
Date Received
February 12, 1993
Decision Date
March 31, 1994
Product Code
ITI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ITI Wheelchair, Powered

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Other Clearances by Pegasus Airwave, Inc.

K Number Device Name
K944310 PEGASUS BIWAVE PLUS SYSTEM
K933004 PEGASUS BIWAVE SYSTEM
K874877 PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER