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FDA 510(k)

NEEDLE/CANNULA

K-Number: K950574 · 1995-02-24

ApplicantTri-Med Specialties, Inc.
Decision Date1995-02-24
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

NEEDLE/CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Med Specialties, Inc.. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K950574. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEEDLE/CANNULA?

NEEDLE/CANNULA is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Tri-Med Specialties, Inc.. The 510(k) number is K950574.

When did NEEDLE/CANNULA receive FDA 510(k) clearance?

NEEDLE/CANNULA received FDA 510(k) clearance on 1995-02-24, under 510(k) number K950574.

Who is the listed applicant for NEEDLE/CANNULA?

The FDA 510(k) record lists Tri-Med Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE/CANNULA?

The FDA product code for NEEDLE/CANNULA is LRO.

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Other records listing Tri-Med Specialties, 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.

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Related Devices (Code: LRO)

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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