Atlas FDA

ALARM SYS FOR NITROUS OXIDE SYS.

FDA 510(k) clearance K771246 · decided 1977-07-15

Clearance details

K-number
K771246
Device name
ALARM SYS FOR NITROUS OXIDE SYS.
Applicant
Star Dental Mfg. Co.
Decision
Substantially Equivalent
Date received
1977-07-11
Decision date
1977-07-15
Days to decision
4 days
Clearance type
Traditional
Product code
ECX
Device class
1
Regulation number
868.2700
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Mchenry, IL, 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
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Intelli-Ox (K143060)Air Liquide Healthcare2015-05-21
OXYTOTE INFINITY SERIES VIPR SYSTEMS (K142149)Western/Scott Fetzer Co.2015-04-17
GRAB 'N GO PLUS, GRAB 'N GO DIGITAL (K132778)Praxair Healthcare Services2014-07-07
EZ-OX PLUS GENERATION II (K131386)Air Liquide Healthcare America2014-03-14
LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706 (K101792)Linde Gas North America, LLC2011-03-18
LINDE INTEGRATED VALVE (LIV) (K063354)Linde Gas Therapeutics2007-04-17
OX-SOX, MODEL C, D, E, (K062300)Pattient Safety Innovations, Llp2006-11-27
EZ-OX PLUS (K053117)Air Liquide Healthcare America2006-04-10
MEDICYL-E-LITE PORTABLE OXYGEN DELIVERY SYSTEM (K033897)Aga-Linde Health Care2004-07-19

Recalls involving this device

No recalls on record reference this clearance.