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FDA 510(k)

SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM

K-Number: K960771 · 1996-12-10

Decision Date1996-12-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rymed Technologies, Inc.. It received FDA 510(k) clearance on 1996-12-10 under 510(k) number K960771. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM?

SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1996-12-10. The listed applicant is Rymed Technologies, Inc.. The 510(k) number is K960771.

When did SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM receive FDA 510(k) clearance?

SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM received FDA 510(k) clearance on 1996-12-10, under 510(k) number K960771.

Who is the listed applicant for SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM?

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

What is the FDA product code for SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM?

The FDA product code for SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEM is FPA.

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 Rymed Technologies, 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.

Related Devices (Code: FPA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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