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FDA 510(k)

COCAINE KIT, TOXI-PAK

K-Number: K760401 · 1976-08-26

ApplicantJ.T. Baker Chemical Co.
Decision Date1976-08-26
Product CodeDLN
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

COCAINE KIT, TOXI-PAK is the device name listed in this FDA 510(k) record. The listed applicant is J.T. Baker Chemical Co.. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760401. The device is classified under product code DLN. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCAINE KIT, TOXI-PAK?

COCAINE KIT, TOXI-PAK is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K760401.

When did COCAINE KIT, TOXI-PAK receive FDA 510(k) clearance?

COCAINE KIT, TOXI-PAK received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760401.

Who is the listed applicant for COCAINE KIT, TOXI-PAK?

The FDA 510(k) record lists J.T. Baker Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COCAINE KIT, TOXI-PAK?

The FDA product code for COCAINE KIT, TOXI-PAK is DLN.

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Other records listing J.T. Baker Chemical Co. as applicant

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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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