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

RHINO-GUARD

K Number: K911785 · Decision Oct 7, 1991
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
29
Review Days
168

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Basic Information

Device Name
RHINO-GUARD
K Number
K911785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Micromedics, Inc.
Date Received
April 22, 1991
Decision Date
October 7, 1991
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

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