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FDA 510(k)

P.A. ENTERAL FEEDING BAG 1100

K-Number: K853309 · 1985-08-27

Decision Date1985-08-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

P.A. ENTERAL FEEDING BAG 1100 is the device name listed in this FDA 510(k) record. The listed applicant is Pa Medical Corp.. It received FDA 510(k) clearance on 1985-08-27 under 510(k) number K853309. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.A. ENTERAL FEEDING BAG 1100?

P.A. ENTERAL FEEDING BAG 1100 is a medical device that received FDA 510(k) clearance on 1985-08-27. The listed applicant is Pa Medical Corp.. The 510(k) number is K853309.

When did P.A. ENTERAL FEEDING BAG 1100 receive FDA 510(k) clearance?

P.A. ENTERAL FEEDING BAG 1100 received FDA 510(k) clearance on 1985-08-27, under 510(k) number K853309.

Who is the listed applicant for P.A. ENTERAL FEEDING BAG 1100?

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

What is the FDA product code for P.A. ENTERAL FEEDING BAG 1100?

The FDA product code for P.A. ENTERAL FEEDING BAG 1100 is KNT.

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 Pa Medical Corp. 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: KNT)

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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