FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

SULLIVAN NOSE & MOUTH MASK SYSTEM

K Number: K952475 · Decision May 28, 1996
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
4
Review Days
364

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Basic Information

Device Name
SULLIVAN NOSE & MOUTH MASK SYSTEM
K Number
K952475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Rescare , Ltd.
Date Received
May 30, 1995
Decision Date
May 28, 1996
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 Rescare , Ltd.

K Number Device Name
K952429 RES CARE AUTO SET CLINICAL, PORTABLE SYSTEM, PORTABLE 2 SYSTEM
K931884 SULLIVAN NASAL VPAP SYSTEM
K930656 SULLIVAN III NASAL CPAP SYSTEM