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FDA 510(k)

COMPRESSOR, AIR, MINI-SILENT

K-Number: K781213 · 1978-07-27

Decision Date1978-07-27
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPRESSOR, AIR, MINI-SILENT is the device name listed in this FDA 510(k) record. The listed applicant is The John Bunn Co.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K781213. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSOR, AIR, MINI-SILENT?

COMPRESSOR, AIR, MINI-SILENT is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is The John Bunn Co.. The 510(k) number is K781213.

When did COMPRESSOR, AIR, MINI-SILENT receive FDA 510(k) clearance?

COMPRESSOR, AIR, MINI-SILENT received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781213.

Who is the listed applicant for COMPRESSOR, AIR, MINI-SILENT?

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

What is the FDA product code for COMPRESSOR, AIR, MINI-SILENT?

The FDA product code for COMPRESSOR, AIR, MINI-SILENT is BTI.

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 The John Bunn Co. 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: BTI)

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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