FDA 510(k)

TEFLON BIOPSY CATHETER W/TIP ANGLE

K-Number: K870734 · 1987-03-10

Decision Date1987-03-10

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

TEFLON BIOPSY CATHETER W/TIP ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1987-03-10 under 510(k) number K870734. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEFLON BIOPSY CATHETER W/TIP ANGLE?

TEFLON BIOPSY CATHETER W/TIP ANGLE is a medical device that received FDA 510(k) clearance on 1987-03-10. The listed applicant is Van-Tec, Inc.. The 510(k) number is K870734.

When did TEFLON BIOPSY CATHETER W/TIP ANGLE receive FDA 510(k) clearance?

TEFLON BIOPSY CATHETER W/TIP ANGLE received FDA 510(k) clearance on 1987-03-10, under 510(k) number K870734.

Who is the listed applicant for TEFLON BIOPSY CATHETER W/TIP ANGLE?

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

What is the FDA product code for TEFLON BIOPSY CATHETER W/TIP ANGLE?

The FDA product code for TEFLON BIOPSY CATHETER W/TIP ANGLE is KNW.

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Other records listing Van-Tec, Inc. as applicant

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Related Devices (Code: KNW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.