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FDA 510(k)

FOREIGN BODY PROTECTOR

K-Number: K841258 · 1984-07-09

Decision Date1984-07-09
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FOREIGN BODY PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Jayco Pharmaceuticals. It received FDA 510(k) clearance on 1984-07-09 under 510(k) number K841258. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOREIGN BODY PROTECTOR?

FOREIGN BODY PROTECTOR is a medical device that received FDA 510(k) clearance on 1984-07-09. The listed applicant is Jayco Pharmaceuticals. The 510(k) number is K841258.

When did FOREIGN BODY PROTECTOR receive FDA 510(k) clearance?

FOREIGN BODY PROTECTOR received FDA 510(k) clearance on 1984-07-09, under 510(k) number K841258.

Who is the listed applicant for FOREIGN BODY PROTECTOR?

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

What is the FDA product code for FOREIGN BODY PROTECTOR?

The FDA product code for FOREIGN BODY PROTECTOR is FED.

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 Jayco Pharmaceuticals 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 9 devices →

Related Devices (Code: FED)

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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