VENOUS CANNULA TRAY— 510(k) K813284

Substantially Equivalent

Cunningham Woodland, Inc.

FDA 510(k) clearance K813284 for VENOUS CANNULA TRAY, Substantially Equivalent on 1981-12-29. Applicant: Cunningham Woodland, Inc.. Device class: 1.

Clearance details

Applicant: Cunningham Woodland, Inc.
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1981-11-23
Decision date: 1981-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DWS

K022238 — MYOCARDIAL LEAD IMPLANT TOOL, MODEL 106262002-10-09
K964445 — OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)1997-01-30
K962771 — BURKE CONGENITAL THORACOSCOPY INSTRUMENTS1996-11-19
K955689 — RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAY1996-05-15
K960139 — G.E. STERILE ANGIOGRAPHIC TRAY1996-04-19

More clearances from Cunningham Woodland, Inc.

K823527 — SUBCLAVIAN INSERTION KIT1983-03-31
K813286 — PRE-PACK TENS1982-01-22
K813519 — NON-ABSORBENT TOWELS1982-01-05
K811088 — DRESSING TRAY MERCY HOSPITAL1981-05-08
K811089 — ONE STEP PREP KIT1981-05-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.