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FDA 510(k)

POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE

K-Number: K872182 · 1987-10-30

ApplicantPolystan C/O Vitalcor, Inc.
Decision Date1987-10-30
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Polystan C/O Vitalcor, Inc.. It received FDA 510(k) clearance on 1987-10-30 under 510(k) number K872182. 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 POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE?

POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Polystan C/O Vitalcor, Inc.. The 510(k) number is K872182.

When did POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE receive FDA 510(k) clearance?

POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE received FDA 510(k) clearance on 1987-10-30, under 510(k) number K872182.

Who is the listed applicant for POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE?

The FDA 510(k) record lists Polystan C/O Vitalcor, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE?

The FDA product code for POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE is DQY.

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Other records listing Polystan C/O Vitalcor, Inc. 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.

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Related Devices (Code: DQY)

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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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