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FDA 510(k)

FLAT SILICONE DRAIN

K-Number: K782026 · 1978-12-12

ApplicantDavol, Inc.
Decision Date1978-12-12
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLAT SILICONE DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1978-12-12 under 510(k) number K782026. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLAT SILICONE DRAIN?

FLAT SILICONE DRAIN is a medical device that received FDA 510(k) clearance on 1978-12-12. The listed applicant is Davol, Inc.. The 510(k) number is K782026.

When did FLAT SILICONE DRAIN receive FDA 510(k) clearance?

FLAT SILICONE DRAIN received FDA 510(k) clearance on 1978-12-12, under 510(k) number K782026.

Who is the listed applicant for FLAT SILICONE DRAIN?

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

What is the FDA product code for FLAT SILICONE DRAIN?

The FDA product code for FLAT SILICONE DRAIN is GCY.

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Other records listing Davol, 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.

K251557Bard® Mesh; Bard® Mesh Pre-ShapedK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedK031213AQUASENS FLUID MONITORING SYSTEMK030307DAVOL ARTHROVENT OUTFLOW TUBINGK003323COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205K003790DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000, 5552001, 552002, 5552003, 5552004, 5552005

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Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

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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