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FDA 510(k)

X-RAY ASSIST BAR

K-Number: K972000 · 1997-07-08

ApplicantRalph Lindel, D.C.
Decision Date1997-07-08
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY ASSIST BAR is the device name listed in this FDA 510(k) record. The listed applicant is Ralph Lindel, D.C.. It received FDA 510(k) clearance on 1997-07-08 under 510(k) number K972000. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY ASSIST BAR?

X-RAY ASSIST BAR is a medical device that received FDA 510(k) clearance on 1997-07-08. The listed applicant is Ralph Lindel, D.C.. The 510(k) number is K972000.

When did X-RAY ASSIST BAR receive FDA 510(k) clearance?

X-RAY ASSIST BAR received FDA 510(k) clearance on 1997-07-08, under 510(k) number K972000.

Who is the listed applicant for X-RAY ASSIST BAR?

The FDA 510(k) record lists Ralph Lindel, D.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY ASSIST BAR?

The FDA product code for X-RAY ASSIST BAR is KPR.

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Related Devices (Code: KPR)

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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