Atlas FDA

POWDER BLOWERS

FDA 510(k) clearance K822351 · decided 1982-09-14

Clearance details

K-number
K822351
Device name
POWDER BLOWERS
Applicant
Kelleher Corp.
Decision
Substantially Equivalent
Date received
1982-08-06
Decision date
1982-09-14
Days to decision
39 days
Clearance type
Traditional
Product code
KMA
Device class
1
Regulation number
874.5550
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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RINOFLOW MICRONIZED E.N.T. WASH SYSTEM (K973875)Respironics, Inc.1998-01-26
RINOFLOW MICRONIZED E.N..T. WASH SYTSTEM (K963550)Respironics, Inc.1996-11-01
MICROFLOW IRRIGATION SYSTEM (K950078)Jedmed Instrument Co.1995-06-21

Recalls involving this device

No recalls on record reference this clearance.