FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ASEPT PLEURAL DRAINAGE SYSTEM

K Number: K093307 · Decision Nov 6, 2009
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
18
Applicant Total
20
Review Days
15

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Basic Information

Device Name
ASEPT PLEURAL DRAINAGE SYSTEM
K Number
K093307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5050
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pfm Medical, Inc.
Date Received
October 22, 2009
Decision Date
November 6, 2009
Product Code
DWM
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
Y

Classifications

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

Product Code Device Name
DWM Apparatus, Suction, Patient Care

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K140137 SAFETY BIOPSY NEEDLE SYSTEM
K122402 LPP (LOW PROFILE PORT)
K113354 VETA PERITONEAL DIALYSIS CATHETER
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