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

SWAN-NECK PERITONEAL DIALYSIS CATHETERS

K Number: K862046 · Decision Jun 19, 1986
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
47
Applicant Total
9
Review Days
21

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Basic Information

Device Name
SWAN-NECK PERITONEAL DIALYSIS CATHETERS
K Number
K862046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Accurate Surgical Instruments Co.
Date Received
May 29, 1986
Decision Date
June 19, 1986
Product Code
FJS
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
FJS Catheter, Peritoneal, Long-Term Indwelling

Similar 510(k) Clearances

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

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Other Clearances by Accurate Surgical Instruments Co.

K Number Device Name
K950042 SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETER
K920515 INSERTION
K910786 TROCAR (FALLER STYLET)
K910785 TITANIUM CATHETER EXTENDER
K910787 TITANIUM CONNECTOR (2 PART)
K850214 STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN
K813488 CATHETER REGULAR
K813487 CATHETER BUBBLE STAND