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FDA 510(k)

ANESTHESIA TRAY, CAUDAL

K-Number: K780120 · 1978-02-06

ApplicantKendall Research Center
Decision Date1978-02-06
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA TRAY, CAUDAL is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Research Center. It received FDA 510(k) clearance on 1978-02-06 under 510(k) number K780120. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA TRAY, CAUDAL?

ANESTHESIA TRAY, CAUDAL is a medical device that received FDA 510(k) clearance on 1978-02-06. The listed applicant is Kendall Research Center. The 510(k) number is K780120.

When did ANESTHESIA TRAY, CAUDAL receive FDA 510(k) clearance?

ANESTHESIA TRAY, CAUDAL received FDA 510(k) clearance on 1978-02-06, under 510(k) number K780120.

Who is the listed applicant for ANESTHESIA TRAY, CAUDAL?

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

What is the FDA product code for ANESTHESIA TRAY, CAUDAL?

The FDA product code for ANESTHESIA TRAY, CAUDAL is CAZ.

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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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