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

TRANSCEND AUTO

K Number: K132127 · Decision Oct 17, 2013
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
3
Review Days
99

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Basic Information

Device Name
TRANSCEND AUTO
K Number
K132127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somnetics International, Inc.
Date Received
July 10, 2013
Decision Date
October 17, 2013
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

Similar 510(k) Clearances

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

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Other Clearances by Somnetics International, Inc.

K Number Device Name
K180388 Transcend 365 miniCPAP System
K131388 TRANSCEND HEATED HUMIDIFIER