TUBE, FEEDING, ARGYLE
K-Number: K760137 · 1976-07-16
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Device Summary
Frequently Asked Questions
What is the TUBE, FEEDING, ARGYLE?
TUBE, FEEDING, ARGYLE is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760137.
When did TUBE, FEEDING, ARGYLE receive FDA 510(k) clearance?
TUBE, FEEDING, ARGYLE received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760137.
Who is the listed applicant for TUBE, FEEDING, ARGYLE?
The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBE, FEEDING, ARGYLE?
The FDA product code for TUBE, FEEDING, ARGYLE is FPD.
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 Industries 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: FPD)
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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