FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

SWABCAP

K Number: K083508 · Decision Apr 28, 2009
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
21
Applicant Total
9
Review Days
153

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Basic Information

Device Name
SWABCAP
K Number
K083508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Excelsior Medical Corp.
Date Received
November 26, 2008
Decision Date
April 28, 2009
Product Code
QBP
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
QBP Cap, Device Disinfectant

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QBP), ordered by most recent decision date.

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Other Clearances by Excelsior Medical Corp.

K Number Device Name
K130975 SWABCAP AND SWABFLUSH
K101270 SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311
K082837 STERILE FIELD SALINE PRE-FILLED SYRINGE(S)
K061497 SYREX HEPARIN LOCK FLUSH SYRINGE, 1 UNIT/ML & 2 UNITS/ML
K053120 STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES
K023740 SYREX PRE-FILLED SYRINGE
K962938 EXCELSIOR DISPOSABLE SYRINGE W/NORMAL SALINE (.9% SODIUM CHLORIDE)
K942349 MICROBORE EXTENSION SET