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FDA 510(k)

SAFETY INJECTION PORT, MODIFICATION

K-Number: K913311 · 1991-09-13

Decision Date1991-09-13
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETY INJECTION PORT, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Riverside Technology, Inc.. It received FDA 510(k) clearance on 1991-09-13 under 510(k) number K913311. 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 SAFETY INJECTION PORT, MODIFICATION?

SAFETY INJECTION PORT, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-09-13. The listed applicant is Riverside Technology, Inc.. The 510(k) number is K913311.

When did SAFETY INJECTION PORT, MODIFICATION receive FDA 510(k) clearance?

SAFETY INJECTION PORT, MODIFICATION received FDA 510(k) clearance on 1991-09-13, under 510(k) number K913311.

Who is the listed applicant for SAFETY INJECTION PORT, MODIFICATION?

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

What is the FDA product code for SAFETY INJECTION PORT, MODIFICATION?

The FDA product code for SAFETY INJECTION PORT, MODIFICATION 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.

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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