TISPORT X AND TISPORT XC
K-Number: K990555 · 1999-03-22
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Device Summary
Frequently Asked Questions
What is the TISPORT X AND TISPORT XC?
TISPORT X AND TISPORT XC is a medical device that received FDA 510(k) clearance on 1999-03-22. The listed applicant is Tisport. The 510(k) number is K990555.
When did TISPORT X AND TISPORT XC receive FDA 510(k) clearance?
TISPORT X AND TISPORT XC received FDA 510(k) clearance on 1999-03-22, under 510(k) number K990555.
Who is the listed applicant for TISPORT X AND TISPORT XC?
The FDA 510(k) record lists Tisport as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TISPORT X AND TISPORT XC?
The FDA product code for TISPORT X AND TISPORT XC is IOR.
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 Tisport 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: IOR)
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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