Atlas FDA

NEO 2 LINE SUCTION SYSTEM

FDA 510(k) clearance K960488 · decided 1996-04-26

Clearance details

K-number
K960488
Device name
NEO 2 LINE SUCTION SYSTEM
Applicant
Alcove Medical, Inc.
Decision
Substantially Equivalent
Date received
1996-02-01
Decision date
1996-04-26
Days to decision
85 days
Clearance type
Traditional
Product code
BSY
Device class
1
Regulation number
868.6810
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEM (K031997)Mallinckrodt Dar S.R.L.2003-11-25
AMBU HAND POWER SUCTION PUMP (K992902)Ambu, Inc.1999-10-25
DUAL PURPOSE CLOSED CATHETER (K982945)Spirit Medical Systems, Inc.1998-09-22
SUCTION CATHETER (K981910)Ni-Med, Inc.1998-08-24
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
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
REDI NURSE SYSTEM (RNS) STERILE WATER FOR IRRIGATION (K952395)Contour Fabricators of Florida, Inc.1995-08-15

Recalls involving this device

No recalls on record reference this clearance.