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FDA 510(k)

VBMAX

K-Number: K000654 · 2000-11-14

ApplicantA-M Systems, Inc.
Decision Date2000-11-14
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VBMAX is the device name listed in this FDA 510(k) record. The listed applicant is A-M Systems, Inc.. It received FDA 510(k) clearance on 2000-11-14 under 510(k) number K000654. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VBMAX?

VBMAX is a medical device that received FDA 510(k) clearance on 2000-11-14. The listed applicant is A-M Systems, Inc.. The 510(k) number is K000654.

When did VBMAX receive FDA 510(k) clearance?

VBMAX received FDA 510(k) clearance on 2000-11-14, under 510(k) number K000654.

Who is the listed applicant for VBMAX?

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

What is the FDA product code for VBMAX?

The FDA product code for VBMAX is CAH.

Related Clinical Trials

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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Other records listing A-M Systems, 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.

K063526A-M SYSTEMS VIROMAX VIRAL AND BACTERIAL FILTER

Related Devices (Code: CAH)

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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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