Atlas FDA

DISPOSABLE MEDICATION NEBULIZER

FDA 510(k) clearance K801867 · decided 1980-08-20

Clearance details

K-number
K801867
Device name
DISPOSABLE MEDICATION NEBULIZER
Applicant
Hospitax
Decision
Substantially Equivalent
Date received
1980-08-05
Decision date
1980-08-20
Days to decision
15 days
Clearance type
Traditional
Product code
LCQ
Device class
2
Regulation number
862.3450
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
VARIANT EXPRESS GLYCOHEMOGLOBIN PROGRAM (K972609)Bio-Rad1997-08-06
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OPUS GENTAMICIN (K905721)Pb Diagnostic Systems, Inc.1991-02-21
'TDXFLX ANALYZER (K904226)Abbott Laboratories1990-10-29
FPR GENTAMICIN KIT (K894523)Colony Laboratories, Inc.1989-09-28
BIOPROBE FLUOR GENTAMICIN IN SERUM OR PLASMA (K852158)Bioprobe Intl., Inc.1985-06-25
GENTAMICIN KIT(FPIA) (K852013)Windsor Laboratories, Inc.1985-06-10
COBAS REAGENTS FOR GENTAMICIN & CALIBRAT (K843827)Roche Diagnostic Systems, Inc.1985-02-01
INNOFLOUR GENTAMICIN (K841865)Innotron Diagnostics1984-05-31
IMMPULSE GENTAMICIN ASSAY REAGENTS (K841162)Paragon Diagnostics, Inc.1984-05-02

Recalls involving this device

RecordFirmDate
Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquid recall (Z-1044-2016)ConvaTec, Inc2016-03-03