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FDA 510(k)

TUBING FEEDING KIT

K-Number: K770620 · 1977-05-03

Decision Date1977-05-03
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBING FEEDING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Doyle Pharmaceutical. It received FDA 510(k) clearance on 1977-05-03 under 510(k) number K770620. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING FEEDING KIT?

TUBING FEEDING KIT is a medical device that received FDA 510(k) clearance on 1977-05-03. The listed applicant is Doyle Pharmaceutical. The 510(k) number is K770620.

When did TUBING FEEDING KIT receive FDA 510(k) clearance?

TUBING FEEDING KIT received FDA 510(k) clearance on 1977-05-03, under 510(k) number K770620.

Who is the listed applicant for TUBING FEEDING KIT?

The FDA 510(k) record lists Doyle Pharmaceutical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUBING FEEDING KIT?

The FDA product code for TUBING FEEDING KIT 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.

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

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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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