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FDA 510(k)

RECEPTAL ATS TRAUMA KGA1900L

K-Number: K772196 · 1977-12-22

ApplicantSorensen Research
Decision Date1977-12-22
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RECEPTAL ATS TRAUMA KGA1900L is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1977-12-22 under 510(k) number K772196. 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 TRAUMA KGA1900L?

RECEPTAL ATS TRAUMA KGA1900L is a medical device that received FDA 510(k) clearance on 1977-12-22. The listed applicant is Sorensen Research. The 510(k) number is K772196.

When did RECEPTAL ATS TRAUMA KGA1900L receive FDA 510(k) clearance?

RECEPTAL ATS TRAUMA KGA1900L received FDA 510(k) clearance on 1977-12-22, under 510(k) number K772196.

Who is the listed applicant for RECEPTAL ATS TRAUMA KGA1900L?

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 TRAUMA KGA1900L?

The FDA product code for RECEPTAL ATS TRAUMA KGA1900L 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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