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FDA 510(k)

MODEL H170 PEDIATRIC CHEST X-RAY UNIT

K-Number: K915667 · 1992-01-31

Decision Date1992-01-31
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL H170 PEDIATRIC CHEST X-RAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is H.L. Lyons Co.. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K915667. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL H170 PEDIATRIC CHEST X-RAY UNIT?

MODEL H170 PEDIATRIC CHEST X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is H.L. Lyons Co.. The 510(k) number is K915667.

When did MODEL H170 PEDIATRIC CHEST X-RAY UNIT receive FDA 510(k) clearance?

MODEL H170 PEDIATRIC CHEST X-RAY UNIT received FDA 510(k) clearance on 1992-01-31, under 510(k) number K915667.

Who is the listed applicant for MODEL H170 PEDIATRIC CHEST X-RAY UNIT?

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

What is the FDA product code for MODEL H170 PEDIATRIC CHEST X-RAY UNIT?

The FDA product code for MODEL H170 PEDIATRIC CHEST X-RAY UNIT is IXY.

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.

Related Devices (Code: IXY)

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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