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

TRANSDUCER FILTER

K Number: K821268 · Decision Jun 23, 1982
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
34
Applicant Total
31
Review Days
51

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Basic Information

Device Name
TRANSDUCER FILTER
K Number
K821268
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Cp Medical
Date Received
May 3, 1982
Decision Date
June 23, 1982
Product Code
FIB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FIB Protector, Transducer, Dialysis

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Other Clearances by Cp Medical

K Number Device Name
K094028 CP-FIBER (ORTHOFIBER)
K072229 MONOSWIFT
K071550 PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS
K060987 OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31
K041894 ORTHOFIBER
K034062 CP SLEEVE AND RIVER SLEEVE
K024372 CP MEDICAL BONE WAX
K030786 MONO-SWIFT
K030351 STAINLESS STEEL SURGICAL SUTURE, NON-ABSORBABLE
K023710 VISORB SWIFT
Search all 31 clearances from Cp Medical →