Atlas FDA

MUCOUS TRAP

FDA 510(k) clearance K896560 · decided 1990-01-22

Clearance details

K-number
K896560
Device name
MUCOUS TRAP
Applicant
Westmark, Sterile Packing Systems, Inc. (Sps)
Decision
Substantially Equivalent
Date received
1989-11-17
Decision date
1990-01-22
Days to decision
66 days
Clearance type
Traditional
Product code
BSY
Device class
1
Regulation number
868.6810
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Grand Rapids, MI, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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AMBU HAND POWER SUCTION PUMP (K992902)Ambu, Inc.1999-10-25
DUAL PURPOSE CLOSED CATHETER (K982945)Spirit Medical Systems, Inc.1998-09-22
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HI-CARE CLOSED SUCTION SYSTEM (K972258)Mallinckrodt Medical1997-12-29
AMSINO SUCTION CATHETER (K973199)Amsino Intl., Inc.1997-09-10
TRACH-EZE CLOSED VENTILATION SUCTION SYSTEM (K961707)Sorenson Critical Care1997-03-11
TRACH CARE SET WITH MICROBAN (K964369)Ballard Medical Products1997-02-11
NEO 2 LINE SUCTION SYSTEM (K960488)Alcove Medical, Inc.1996-04-26
ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM (K955831)Sherwood Medical Co.1996-03-28
CATH-GUIDE (K955645)Hudson Respiratory Care, Inc.1996-03-12
REDI NURSE SYSTEM (RNS) STERILE 0.9% SODIUM CHLORIDE SOLUTION (K952396)Contour Fabricators of Florida, Inc.1995-08-15

Recalls involving this device

No recalls on record reference this clearance.