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

DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)

K Number: K953206 · Decision Aug 28, 1995
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
11
Review Days
90

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Basic Information

Device Name
DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)
K Number
K953206
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dhd Diemolding Healthcare Div.
Date Received
May 30, 1995
Decision Date
August 28, 1995
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)

Similar 510(k) Clearances

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

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Other Clearances by Dhd Diemolding Healthcare Div.

K Number Device Name
K973532 STEALTH, METERED DOSE INHALER (MDI) SPACER WITHOUT INTEGRAL ACTUATOR
K970596 DHD EMERALD PRODUCT
K961973 DHD ACE WITH MASK KIT
K945118 EXPIRATORY BREATHING EXERCISER
K944900 THERAPEP
K926301 ACE AEROSOL ENHANCER, HAND HELD ORAL INHALATION CO
K922537 DURALIFE
K913726 DURALIFE(TM)
K913326 DHD METERED DOSE INHALER (MDI) SPACER
K911294 ULTRASET CATHETER
Search all 11 clearances from Dhd Diemolding Healthcare Div. →