Atlas FDA

SILCATH CENTRAL CATHETER TRAY SIZE-

FDA 510(k) clearance K831451 · decided 1983-06-08

Clearance details

K-number
K831451
Device name
SILCATH CENTRAL CATHETER TRAY SIZE-
Applicant
Argon Medical Corp.
Decision
Substantially Equivalent
Date received
1983-05-05
Decision date
1983-06-08
Days to decision
34 days
Clearance type
Traditional
Product code
JCY
Device class
1
Regulation number
878.4200
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY (K863982)Vas-Cath of Canada , Ltd.1986-10-24
SILICONE SUMP DRAIN 20 & 40 FRENCH (K840324)Superior Plastic Products Corp.1984-04-25
TRIPLE LUMEN INFUSIONCATHETERS- (K834615)Medical Components, Inc.1984-02-14
SILCATH CENTRAL CATHETER TRAY W/18 GA (K831453)Argon Medical Corp.1983-07-28
CHEMOTHERAPY INFUSION CATHETER (K822096)American Heyer Schulte1983-04-12
SILICONE ELASTOMER INFUSION CATHETER (K813606)Quest Medical, Inc.1982-01-18
JELCO & KVO CATHETER PLACEMENT UNIT (K791372)Jelco Laboratories1979-09-12
CATHETER, CEBTRAL VENOUS, 2N1501 (K771861)Travenol Laboratories, S.A.1977-11-28
CATHETER, INTRAVASCULAR (ARGYLE IV SK) (K760760)Sherwood Medical Industries1976-12-09
CATHETER, VEIN (BRAUNULA) (K760391)B. Braun Instruments1976-11-02
INTRAVENOUS TRANSFER SET (INTRAFIX) (K760380)B. Braun Instruments1976-11-02
BLOOD TRANSFUSION SET (SANGOFIX) (K760381)B. Braun Instruments1976-11-02

Recalls involving this device

No recalls on record reference this clearance.