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FDA 510(k)

KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT

K-Number: K953980 · 1995-11-16

ApplicantKreuzer Corp.
Decision Date1995-11-16
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT is the device name listed in this FDA 510(k) record. The listed applicant is Kreuzer Corp.. It received FDA 510(k) clearance on 1995-11-16 under 510(k) number K953980. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT?

KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT is a medical device that received FDA 510(k) clearance on 1995-11-16. The listed applicant is Kreuzer Corp.. The 510(k) number is K953980.

When did KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT receive FDA 510(k) clearance?

KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT received FDA 510(k) clearance on 1995-11-16, under 510(k) number K953980.

Who is the listed applicant for KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT?

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

What is the FDA product code for KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT?

The FDA product code for KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT is FQO.

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Related Devices (Code: FQO)

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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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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