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FDA 510(k)

RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS

K-Number: K884435 · 1988-11-08

Decision Date1988-11-08
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Connections, Inc.. It received FDA 510(k) clearance on 1988-11-08 under 510(k) number K884435. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS?

RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Clinical Connections, Inc.. The 510(k) number is K884435.

When did RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS receive FDA 510(k) clearance?

RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS received FDA 510(k) clearance on 1988-11-08, under 510(k) number K884435.

Who is the listed applicant for RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS?

The FDA 510(k) record lists Clinical Connections, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS?

The FDA product code for RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS is FMG.

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 Clinical Connections, Inc. 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 10 devices →

Related Devices (Code: FMG)

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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