TISSU TRANS HARVEST TUBING
K-Number: K092022 · 2009-08-17
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Device Summary
Frequently Asked Questions
What is the TISSU TRANS HARVEST TUBING?
TISSU TRANS HARVEST TUBING is a medical device that received FDA 510(k) clearance on 2009-08-17. The listed applicant is Shippert Medical Technologies Corp.. The 510(k) number is K092022.
When did TISSU TRANS HARVEST TUBING receive FDA 510(k) clearance?
TISSU TRANS HARVEST TUBING received FDA 510(k) clearance on 2009-08-17, under 510(k) number K092022.
Who is the listed applicant for TISSU TRANS HARVEST TUBING?
The FDA 510(k) record lists Shippert Medical Technologies Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TISSU TRANS HARVEST TUBING?
The FDA product code for TISSU TRANS HARVEST TUBING is KYZ.
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 Shippert Medical Technologies Corp. 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: KYZ)
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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