ARGYLE VAC-U-CARE FLAT SILICONE WOUND T.
K-Number: K801371 · 1980-06-26
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Device Summary
Frequently Asked Questions
What is the ARGYLE VAC-U-CARE FLAT SILICONE WOUND T.?
ARGYLE VAC-U-CARE FLAT SILICONE WOUND T. is a medical device that received FDA 510(k) clearance on 1980-06-26. The listed applicant is Sherwood Medical Co.. The 510(k) number is K801371.
When did ARGYLE VAC-U-CARE FLAT SILICONE WOUND T. receive FDA 510(k) clearance?
ARGYLE VAC-U-CARE FLAT SILICONE WOUND T. received FDA 510(k) clearance on 1980-06-26, under 510(k) number K801371.
Who is the listed applicant for ARGYLE VAC-U-CARE FLAT SILICONE WOUND T.?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARGYLE VAC-U-CARE FLAT SILICONE WOUND T.?
The FDA product code for ARGYLE VAC-U-CARE FLAT SILICONE WOUND T. 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 Sherwood Medical Co. 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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