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FDA 510(k)

VAP 2001

K-Number: K801181 · 1981-04-14

ApplicantBlendette Intl. , Ltd.
Decision Date1981-04-14
Product Code
DecisionSubstantially Equivalent

Device Summary

VAP 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Blendette Intl. , Ltd.. It received FDA 510(k) clearance on 1981-04-14 under 510(k) number K801181. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAP 2001?

VAP 2001 is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Blendette Intl. , Ltd.. The 510(k) number is K801181.

When did VAP 2001 receive FDA 510(k) clearance?

VAP 2001 received FDA 510(k) clearance on 1981-04-14, under 510(k) number K801181.

Who is the listed applicant for VAP 2001?

The FDA 510(k) record lists Blendette Intl. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

Other records listing Blendette Intl. , Ltd. 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.

K800366SOLARIUM, MODEL 6040A

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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