Atlas FDA

DELTA T

FDA 510(k) clearance K041076 · decided 2004-08-09

Clearance details

K-number
K041076
Device name
DELTA T
Applicant
Penlon , Ltd.
Decision
Substantially Equivalent
Date received
2004-04-26
Decision date
2004-08-09
Days to decision
105 days
Clearance type
Special
Product code
CAD
Device class
2
Regulation number
868.5880
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Abingdon, GB
Third-party review
No
Expedited review
No

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GAV - GENERAL ANAESTHETIC VAPORIZER (K051666)General Anaesthetic Services Limited2005-08-23
D-VAPOR (K042276)Draeger Medical, Inc.2004-09-23
DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER (ENFLURANE) (K031027)Datex-Ohmeda, Inc.2003-06-26
DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER (K012924)Datex-Ohmeda, Inc.2002-01-30
SIGMA DELTA (K002343)Penlon , Ltd.2001-06-08
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Recalls involving this device

No recalls on record reference this clearance.