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

PATIENT BREATHING CIRCUIT

K Number: K853487 · Decision Sep 6, 1985
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
20
Review Days
17

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Basic Information

Device Name
PATIENT BREATHING CIRCUIT
K Number
K853487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Infrasonics Corp.
Date Received
August 20, 1985
Decision Date
September 6, 1985
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)

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Other Clearances by Infrasonics Corp.

K Number Device Name
K943106 ADULT VENTILATOR
K952878 OXY/STAR LOW FLOW BLENDER
K934753 STAR BREATHING CIRCUITS
K922654 VENTILATOR ADULT STAR MODIFICATION
K923704 INFANT STAR SERIES 500
K922477 MODEL 105 VENTILATOR, MODIFICATION
K920954 AIR STAR
K911804 INFRASONICS VENTILATOR ADULT STAR, MODIFICATION
K913972 STAR SYNC, MODIFICATION
K905272 ADULT STAR, MODIFICATION
Search all 20 clearances from Infrasonics Corp. →