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FDA 510(k)

TRAY, ICED INJECTABLE (26420)

K-Number: K760066 · 1976-07-21

ApplicantInstrumentation Laboratory CO
Decision Date1976-07-21
Product CodeDXL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRAY, ICED INJECTABLE (26420) is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1976-07-21 under 510(k) number K760066. The device is classified under product code DXL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY, ICED INJECTABLE (26420)?

TRAY, ICED INJECTABLE (26420) is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760066.

When did TRAY, ICED INJECTABLE (26420) receive FDA 510(k) clearance?

TRAY, ICED INJECTABLE (26420) received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760066.

Who is the listed applicant for TRAY, ICED INJECTABLE (26420)?

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

What is the FDA product code for TRAY, ICED INJECTABLE (26420)?

The FDA product code for TRAY, ICED INJECTABLE (26420) is DXL.

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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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