INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM
K-Number: K991653 · 1999-06-24
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Device Summary
Frequently Asked Questions
What is the INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM?
INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-24. The listed applicant is Rymed Technologies, Inc.. The 510(k) number is K991653.
When did INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM receive FDA 510(k) clearance?
INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM received FDA 510(k) clearance on 1999-06-24, under 510(k) number K991653.
Who is the listed applicant for INVISION-PLUS 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 INVISION-PLUS INJECTION PORT CONNECTOR SYSTEM?
The FDA product code for INVISION-PLUS 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
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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