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FDA 510(k)

ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION

K-Number: K852914 · 1985-09-25

ApplicantNorton Performance Plastics Corp.
Decision Date1985-09-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1985-09-25 under 510(k) number K852914. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION?

ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION is a medical device that received FDA 510(k) clearance on 1985-09-25. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K852914.

When did ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION receive FDA 510(k) clearance?

ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION received FDA 510(k) clearance on 1985-09-25, under 510(k) number K852914.

Who is the listed applicant for ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION?

The FDA 510(k) record lists Norton Performance Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION?

The FDA product code for ANGIOGRAPHIC, WEDGE PRESS, DUAL THERMOD & INFUSION is DQY.

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Other records listing Norton Performance Plastics Corp. as applicant

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Related Devices (Code: DQY)

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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