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FDA 510(k)

PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER

K-Number: K897075 · 1990-04-10

ApplicantPioneering Technologies, Inc.
Decision Date1990-04-10
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Pioneering Technologies, Inc.. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K897075. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER?

PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Pioneering Technologies, Inc.. The 510(k) number is K897075.

When did PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER receive FDA 510(k) clearance?

PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER received FDA 510(k) clearance on 1990-04-10, under 510(k) number K897075.

Who is the listed applicant for PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER?

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

What is the FDA product code for PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER?

The FDA product code for PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER is DXC.

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Related Devices (Code: DXC)

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.

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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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