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FDA 510(k)

SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT

K-Number: K760448 · 1976-08-27

ApplicantInstrumentation Laboratory CO
Decision Date1976-08-27
Product CodeDXL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT 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 1976-08-27 under 510(k) number K760448. 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 SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT?

SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT is a medical device that received FDA 510(k) clearance on 1976-08-27. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760448.

When did SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT receive FDA 510(k) clearance?

SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT received FDA 510(k) clearance on 1976-08-27, under 510(k) number K760448.

Who is the listed applicant for SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT?

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 SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT?

The FDA product code for SYRINGE, CO2 DRIVEN, IL AUTOMATIC INJECT 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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