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FDA 510(k)

ARGYLE ENTERNAL FEEDING BAG W/ADMIN

K-Number: K840877 · 1984-06-28

Decision Date1984-06-28
Product CodeHFS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARGYLE ENTERNAL FEEDING BAG W/ADMIN is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1984-06-28 under 510(k) number K840877. The device is classified under product code HFS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE ENTERNAL FEEDING BAG W/ADMIN?

ARGYLE ENTERNAL FEEDING BAG W/ADMIN is a medical device that received FDA 510(k) clearance on 1984-06-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K840877.

When did ARGYLE ENTERNAL FEEDING BAG W/ADMIN receive FDA 510(k) clearance?

ARGYLE ENTERNAL FEEDING BAG W/ADMIN received FDA 510(k) clearance on 1984-06-28, under 510(k) number K840877.

Who is the listed applicant for ARGYLE ENTERNAL FEEDING BAG W/ADMIN?

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 ENTERNAL FEEDING BAG W/ADMIN?

The FDA product code for ARGYLE ENTERNAL FEEDING BAG W/ADMIN is HFS.

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.

View all 191 devices →

Related Devices (Code: HFS)

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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