Atlas FDA

MERCURY CPAP

FDA 510(k) clearance K090710 · decided 2009-08-20

Clearance details

K-number
K090710
Device name
MERCURY CPAP
Applicant
Mercury Medical
Decision
Substantially Equivalent
Date received
2009-03-18
Decision date
2009-08-20
Days to decision
155 days
Clearance type
Traditional
Product code
BYE
Device class
2
Regulation number
868.5965
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Bonita Springs, FL, US
Third-party review
No
Expedited review
No

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VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310 (K092029)Draeger Medical AG & Co. KG2010-08-06
BABI*PLUS BUBBLE PAP VALVE (K090317)A Plus Medical2009-05-20
MERCURY MEDICAL PEEP VALVE (K081266)Mercury Enterprizes Dba Mercury Medical2009-03-05
PULMODYNE CHF FLOW GENERATOR SYSTEM (K080256)Pulmodyne2008-05-09
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Recalls involving this device

No recalls on record reference this clearance.