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FDA 510(k)

RECEPTAL ATS MEDIASTINAL LINER

K-Number: K772280 · 1978-01-03

ApplicantSorensen Research
Decision Date1978-01-03
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RECEPTAL ATS MEDIASTINAL LINER is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772280. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECEPTAL ATS MEDIASTINAL LINER?

RECEPTAL ATS MEDIASTINAL LINER is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Sorensen Research. The 510(k) number is K772280.

When did RECEPTAL ATS MEDIASTINAL LINER receive FDA 510(k) clearance?

RECEPTAL ATS MEDIASTINAL LINER received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772280.

Who is the listed applicant for RECEPTAL ATS MEDIASTINAL LINER?

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

What is the FDA product code for RECEPTAL ATS MEDIASTINAL LINER?

The FDA product code for RECEPTAL ATS MEDIASTINAL LINER is CAC.

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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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