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FDA 510(k)

DAVOL SILICONE SHEATH SUMP DRAIN

K-Number: K810158 · 1981-02-13

Decision Date1981-02-13
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVOL SILICONE SHEATH SUMP DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1981-02-13 under 510(k) number K810158. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL SILICONE SHEATH SUMP DRAIN?

DAVOL SILICONE SHEATH SUMP DRAIN is a medical device that received FDA 510(k) clearance on 1981-02-13. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K810158.

When did DAVOL SILICONE SHEATH SUMP DRAIN receive FDA 510(k) clearance?

DAVOL SILICONE SHEATH SUMP DRAIN received FDA 510(k) clearance on 1981-02-13, under 510(k) number K810158.

Who is the listed applicant for DAVOL SILICONE SHEATH SUMP DRAIN?

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

What is the FDA product code for DAVOL SILICONE SHEATH SUMP DRAIN?

The FDA product code for DAVOL SILICONE SHEATH SUMP DRAIN is GBS.

Related Clinical Trials

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.

Other records listing C.R. Bard, 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.

View all 616 devices →

Related Devices (Code: GBS)

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.

Official Source

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

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