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

MICRO MIST(TM) NEBULIZER

K Number: K930525 · Decision Sep 29, 1993
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
15
Review Days
239

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Basic Information

Device Name
MICRO MIST(TM) NEBULIZER
K Number
K930525
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hudson Respiratory Care, Inc.
Date Received
February 2, 1993
Decision Date
September 29, 1993
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 Hudson Respiratory Care, Inc.

K Number Device Name
K031383 MODEL 780
K011134 OXYGEN SUPPLY TUBING, MODEL 1115
K011125 NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCI
K010402 SMOOTH-FLO CIRCUIT
K001213 CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60
K993355 HUDSON RCI CONCHA COLUMN, CAT. NO. 385-40 AND HUDSON RCI CIRCUIT, CAT. NO. 780-40, 780-41, 780-42, 780-43
K994352 SIDE DRAFT NEB-U-MIST NEBULIZER, MODEL 41896
K964719 HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR
K961150 DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA
K961914 BACTERIA/VIRAL FILTER
Search all 15 clearances from Hudson Respiratory Care, Inc. →