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FDA 510(k)

RFS VACUUM GAUGE SCAVENGING CIRCUIT

K-Number: K033503 · 2004-03-12

Decision Date2004-03-12
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RFS VACUUM GAUGE SCAVENGING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Accutron, Inc.. It received FDA 510(k) clearance on 2004-03-12 under 510(k) number K033503. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RFS VACUUM GAUGE SCAVENGING CIRCUIT?

RFS VACUUM GAUGE SCAVENGING CIRCUIT is a medical device that received FDA 510(k) clearance on 2004-03-12. The listed applicant is Accutron, Inc.. The 510(k) number is K033503.

When did RFS VACUUM GAUGE SCAVENGING CIRCUIT receive FDA 510(k) clearance?

RFS VACUUM GAUGE SCAVENGING CIRCUIT received FDA 510(k) clearance on 2004-03-12, under 510(k) number K033503.

Who is the listed applicant for RFS VACUUM GAUGE SCAVENGING CIRCUIT?

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

What is the FDA product code for RFS VACUUM GAUGE SCAVENGING CIRCUIT?

The FDA product code for RFS VACUUM GAUGE SCAVENGING CIRCUIT is CBN.

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.

Other records listing Accutron, 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.

Related Devices (Code: CBN)

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.

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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