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FDA 510(k)

STOPCOCK (ONE-PORT MANIFOLD)

K-Number: K934123 · 1993-11-23

ApplicantMerit Medical Systems, Inc.
Decision Date1993-11-23
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOPCOCK (ONE-PORT MANIFOLD) is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-11-23 under 510(k) number K934123. 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 STOPCOCK (ONE-PORT MANIFOLD)?

STOPCOCK (ONE-PORT MANIFOLD) is a medical device that received FDA 510(k) clearance on 1993-11-23. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K934123.

When did STOPCOCK (ONE-PORT MANIFOLD) receive FDA 510(k) clearance?

STOPCOCK (ONE-PORT MANIFOLD) received FDA 510(k) clearance on 1993-11-23, under 510(k) number K934123.

Who is the listed applicant for STOPCOCK (ONE-PORT MANIFOLD)?

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

What is the FDA product code for STOPCOCK (ONE-PORT MANIFOLD)?

The FDA product code for STOPCOCK (ONE-PORT MANIFOLD) is DTL.

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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.

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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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