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FDA 510(k)

SILICONE SURGICAL VESSEL LOOPS

K-Number: K791370 · 1979-08-03

ApplicantConphar, Inc.
Decision Date1979-08-03
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SILICONE SURGICAL VESSEL LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791370. 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 SILICONE SURGICAL VESSEL LOOPS?

SILICONE SURGICAL VESSEL LOOPS is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Conphar, Inc.. The 510(k) number is K791370.

When did SILICONE SURGICAL VESSEL LOOPS receive FDA 510(k) clearance?

SILICONE SURGICAL VESSEL LOOPS received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791370.

Who is the listed applicant for SILICONE SURGICAL VESSEL LOOPS?

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

What is the FDA product code for SILICONE SURGICAL VESSEL LOOPS?

The FDA product code for SILICONE SURGICAL VESSEL LOOPS is DWS.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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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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