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FDA 510(k)

3-WAY STOPCOCK W/MALE LOCKING LUER ADA.

K-Number: K791914 · 1979-10-11

ApplicantAbbott Laboratories
Decision Date1979-10-11
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3-WAY STOPCOCK W/MALE LOCKING LUER ADA. is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-10-11 under 510(k) number K791914. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.?

3-WAY STOPCOCK W/MALE LOCKING LUER ADA. is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Abbott Laboratories. The 510(k) number is K791914.

When did 3-WAY STOPCOCK W/MALE LOCKING LUER ADA. receive FDA 510(k) clearance?

3-WAY STOPCOCK W/MALE LOCKING LUER ADA. received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791914.

Who is the listed applicant for 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.?

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

What is the FDA product code for 3-WAY STOPCOCK W/MALE LOCKING LUER ADA.?

The FDA product code for 3-WAY STOPCOCK W/MALE LOCKING LUER ADA. is DTL.

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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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