SPONGE, RICHARDS WOUND DRAINAGE SYSTEM
K-Number: K760257 · 1976-08-09
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Device Summary
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.
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
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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