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FDA 510(k)

TOP THREE WAY STOPCOCK

K-Number: K832625 · 1983-10-19

Decision Date1983-10-19
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TOP THREE WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Top Surgical Manufacturers Co.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K832625. 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 TOP THREE WAY STOPCOCK?

TOP THREE WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Top Surgical Manufacturers Co.. The 510(k) number is K832625.

When did TOP THREE WAY STOPCOCK receive FDA 510(k) clearance?

TOP THREE WAY STOPCOCK received FDA 510(k) clearance on 1983-10-19, under 510(k) number K832625.

Who is the listed applicant for TOP THREE WAY STOPCOCK?

The FDA 510(k) record lists Top Surgical Manufacturers Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOP THREE WAY STOPCOCK?

The FDA product code for TOP THREE WAY STOPCOCK is DTL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Top Surgical Manufacturers Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 12 devices →

Related Devices (Code: DTL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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