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FDA 510(k)

THE HILL ADJUSTABLE HA90C

K-Number: K952359 · 1995-06-22

ApplicantHill Laboratories Co.
Decision Date1995-06-22
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE HILL ADJUSTABLE HA90C is the device name listed in this FDA 510(k) record. The listed applicant is Hill Laboratories Co.. It received FDA 510(k) clearance on 1995-06-22 under 510(k) number K952359. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE HILL ADJUSTABLE HA90C?

THE HILL ADJUSTABLE HA90C is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Hill Laboratories Co.. The 510(k) number is K952359.

When did THE HILL ADJUSTABLE HA90C receive FDA 510(k) clearance?

THE HILL ADJUSTABLE HA90C received FDA 510(k) clearance on 1995-06-22, under 510(k) number K952359.

Who is the listed applicant for THE HILL ADJUSTABLE HA90C?

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

What is the FDA product code for THE HILL ADJUSTABLE HA90C?

The FDA product code for THE HILL ADJUSTABLE HA90C is INQ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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