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FDA 510(k)

PFM-90 CEILING TUBE SUPPORT

K-Number: K900234 · 1990-02-26

Decision Date1990-02-26
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PFM-90 CEILING TUBE SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1990-02-26 under 510(k) number K900234. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFM-90 CEILING TUBE SUPPORT?

PFM-90 CEILING TUBE SUPPORT is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K900234.

When did PFM-90 CEILING TUBE SUPPORT receive FDA 510(k) clearance?

PFM-90 CEILING TUBE SUPPORT received FDA 510(k) clearance on 1990-02-26, under 510(k) number K900234.

Who is the listed applicant for PFM-90 CEILING TUBE SUPPORT?

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

What is the FDA product code for PFM-90 CEILING TUBE SUPPORT?

The FDA product code for PFM-90 CEILING TUBE SUPPORT is IYB.

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 Fischer Imaging Corp. 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: IYB)

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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