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FDA 510(k)

CELESTIN PULSION ESOPHOGEAL PROSTHESIS

K-Number: K813169 · 1981-12-03

ApplicantInmed Corp.
Decision Date1981-12-03
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CELESTIN PULSION ESOPHOGEAL PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1981-12-03 under 510(k) number K813169. 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 CELESTIN PULSION ESOPHOGEAL PROSTHESIS?

CELESTIN PULSION ESOPHOGEAL PROSTHESIS is a medical device that received FDA 510(k) clearance on 1981-12-03. The listed applicant is Inmed Corp.. The 510(k) number is K813169.

When did CELESTIN PULSION ESOPHOGEAL PROSTHESIS receive FDA 510(k) clearance?

CELESTIN PULSION ESOPHOGEAL PROSTHESIS received FDA 510(k) clearance on 1981-12-03, under 510(k) number K813169.

Who is the listed applicant for CELESTIN PULSION ESOPHOGEAL PROSTHESIS?

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

What is the FDA product code for CELESTIN PULSION ESOPHOGEAL PROSTHESIS?

The FDA product code for CELESTIN PULSION ESOPHOGEAL PROSTHESIS is KNT.

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Other records listing Inmed Corp. as applicant

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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.

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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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