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FDA 510(k)

VANCE MALLEABLE TIP FILIFORM

K-Number: K792219 · 1979-12-06

ApplicantVance Products, Inc.
Decision Date1979-12-06
Product CodeKOE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VANCE MALLEABLE TIP FILIFORM is the device name listed in this FDA 510(k) record. The listed applicant is Vance Products, Inc.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792219. The device is classified under product code KOE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANCE MALLEABLE TIP FILIFORM?

VANCE MALLEABLE TIP FILIFORM is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Vance Products, Inc.. The 510(k) number is K792219.

When did VANCE MALLEABLE TIP FILIFORM receive FDA 510(k) clearance?

VANCE MALLEABLE TIP FILIFORM received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792219.

Who is the listed applicant for VANCE MALLEABLE TIP FILIFORM?

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

What is the FDA product code for VANCE MALLEABLE TIP FILIFORM?

The FDA product code for VANCE MALLEABLE TIP FILIFORM is KOE.

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Other records listing Vance Products, 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: KOE)

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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