JELCO & KVO CATHETER PLACEMENT UNIT— 510(k) K791372

Name: FDA 510(k) clearance K791372
Creator: U.S. Food and Drug Administration
Published: 1979-09-12

Substantially Equivalent

Jelco Laboratories

FDA 510(k) clearance K791372 for JELCO & KVO CATHETER PLACEMENT UNIT, Substantially Equivalent on 1979-09-12. Applicant: Jelco Laboratories. Device class: 1.

Clearance details

Applicant: Jelco Laboratories
Product code: Code JCY
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1979-07-24
Decision date: 1979-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K831453 — SILCATH CENTRAL CATHETER TRAY W/18 GA1983-07-28
K831451 — SILCATH CENTRAL CATHETER TRAY SIZE-1983-06-08

More clearances from Jelco Laboratories

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K791918 — JELCO WINGED INTRAVASCULAR CATHETER1979-10-02
K790967 — CATHETER METAL HUB/RADIOPAQUE1979-06-27
K790968 — CATHETER METAL HUB/NONRADIOPAQUE1979-06-11
K790471 — JELCO* DISC FILTER-0.2 MICRON1979-04-30
K790186 — PROTECTIVSTABILIZER1979-02-26

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