FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

DELTA T

K Number: K041076 · Decision Aug 9, 2004
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
56
Applicant Total
9
Review Days
105

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Basic Information

Device Name
DELTA T
K Number
K041076
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5880
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Penlon , Ltd.
Date Received
April 26, 2004
Decision Date
August 9, 2004
Product Code
CAD
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAD Vaporizer, Anesthesia, Non-Heated

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K002343 SIGMA DELTA
K961468 QUIK-FIL VAPORIZER KEYED FILLER
K960944 PPV VAPORIZER (MODIFICATION)
K953179 CLM LARYNGOSCOPE
K942545 SIGMA ELITE