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FDA 510(k)

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM

K-Number: K760257 · 1976-08-09

Decision Date1976-08-09
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1976-08-09 under 510(k) number K760257. 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 SPONGE, RICHARDS WOUND DRAINAGE SYSTEM?

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K760257.

When did SPONGE, RICHARDS WOUND DRAINAGE SYSTEM receive FDA 510(k) clearance?

SPONGE, RICHARDS WOUND DRAINAGE SYSTEM received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760257.

Who is the listed applicant for SPONGE, RICHARDS WOUND DRAINAGE SYSTEM?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPONGE, RICHARDS WOUND DRAINAGE SYSTEM?

The FDA product code for SPONGE, RICHARDS WOUND DRAINAGE SYSTEM is GCY.

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 Richard'S Medical Equip., 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 48 devices →

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.

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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