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

DUAL SPRAY MINISPACER

K Number: K955805 · Decision Mar 21, 1996
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
15
Review Days
90

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Basic Information

Device Name
DUAL SPRAY MINISPACER
K Number
K955805
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thayer Medical Corp.
Date Received
December 22, 1995
Decision Date
March 21, 1996
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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Other Clearances by Thayer Medical Corp.

K Number Device Name
K102658 MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONS
K993101 LITEAIRE
K992722 PRIMEAIRE
K972237 HAND HELD MEDISPACER
K941026 THAYER MASK TO MOUTHPIECE ADAPTER/CONNECTOR
K924535 THAYER HAND HELD M.K.I. HOLDING CHAMBER
K914283 THAYER EXPANSION CHAMBER METERED DOSE INHALER
K904917 THAYER MIP ADAPTER
K901739 THAYER METERED DOSE INHALER DISPENSER/ADAPTER
K900047 THAYER SUCTION EVACUATION CONDENSATE COLLECTION
Search all 15 clearances from Thayer Medical Corp. →