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FDA 510(k)

PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP

K-Number: K882981 · 1988-09-27

ApplicantPioneering Technologies, Inc.
Decision Date1988-09-27
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP 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 1988-09-27 under 510(k) number K882981. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP?

PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP is a medical device that received FDA 510(k) clearance on 1988-09-27. The listed applicant is Pioneering Technologies, Inc.. The 510(k) number is K882981.

When did PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP receive FDA 510(k) clearance?

PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP received FDA 510(k) clearance on 1988-09-27, under 510(k) number K882981.

Who is the listed applicant for PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP?

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 CORONARY ARTERY RETRACTION CLIP?

The FDA product code for PTI INTRA-ART CORONARY ARTERY RETRACTION CLIP is DWS.

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Other records listing Pioneering Technologies, Inc. as applicant

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Related Devices (Code: DWS)

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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