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FDA 510(k)

VENTEX-IA

K-Number: K864641 · 1987-01-28

ApplicantVentech Corp.
Decision Date1987-01-28
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VENTEX-IA is the device name listed in this FDA 510(k) record. The listed applicant is Ventech Corp.. It received FDA 510(k) clearance on 1987-01-28 under 510(k) number K864641. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTEX-IA?

VENTEX-IA is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is Ventech Corp.. The 510(k) number is K864641.

When did VENTEX-IA receive FDA 510(k) clearance?

VENTEX-IA received FDA 510(k) clearance on 1987-01-28, under 510(k) number K864641.

Who is the listed applicant for VENTEX-IA?

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

What is the FDA product code for VENTEX-IA?

The FDA product code for VENTEX-IA is IKN.

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Related Devices (Code: IKN)

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

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

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