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FDA 510(k)

VENOUS CANNULA TRAY

K-Number: K813284 · 1981-12-29

ApplicantCunningham Woodland, Inc.
Decision Date1981-12-29
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENOUS CANNULA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Cunningham Woodland, Inc.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813284. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOUS CANNULA TRAY?

VENOUS CANNULA TRAY is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Cunningham Woodland, Inc.. The 510(k) number is K813284.

When did VENOUS CANNULA TRAY receive FDA 510(k) clearance?

VENOUS CANNULA TRAY received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813284.

Who is the listed applicant for VENOUS CANNULA TRAY?

The FDA 510(k) record lists Cunningham Woodland, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENOUS CANNULA TRAY?

The FDA product code for VENOUS CANNULA TRAY is DWS.

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Other records listing Cunningham Woodland, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K823527SUBCLAVIAN INSERTION KITK813286PRE-PACK TENSK813519NON-ABSORBENT TOWELSK811090MAJOR DRESSING TRAYK811091MINOR DRESSING TRAYK811089ONE STEP PREP KIT

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Related Devices (Code: DWS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical Systems

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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