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

CANNULA, ARTERY, RENAL

K Number: K780079 · Decision Feb 13, 1978
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
24
Applicant Total
16
Review Days
28

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Basic Information

Device Name
CANNULA, ARTERY, RENAL
K Number
K780079
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Dravon Medical, Inc.
Date Received
January 16, 1978
Decision Date
February 13, 1978
Product Code
DQR
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQR Cannula, Catheter

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Other Clearances by Dravon Medical, Inc.

K Number Device Name
K873455 S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS
K860770 AM-100 I/A AMPAC
K832739 STEDIFLO INFUSION SET
K831842 DRAVON T CLAMP
K812771 PERITONEAL DIALYSIS DRAINAGE
K812772 PERITONEAL DIALYSIS CYCLER SET (8UNIT)
K811851 S-610 SHUNT ADAPTOR SET
K800435 HEMOSTATIC/TUBE OCCLUDING FORCEPS
K782057 CATHETER, RADIOPAQUE TENCKHOFF
K782058 CATHETER, BETA-CAP-PERITONEAL
Search all 16 clearances from Dravon Medical, Inc. →