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FDA 510(k)

SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR

K-Number: K950284 · 1995-05-23

ApplicantSims Deltec, Inc.
Decision Date1995-05-23
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Sims Deltec, Inc.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K950284. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR?

SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Sims Deltec, Inc.. The 510(k) number is K950284.

When did SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR receive FDA 510(k) clearance?

SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR received FDA 510(k) clearance on 1995-05-23, under 510(k) number K950284.

Who is the listed applicant for SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR?

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

What is the FDA product code for SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR?

The FDA product code for SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR is FOZ.

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Other records listing Sims Deltec, Inc. as applicant

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Related Devices (Code: FOZ)

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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