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FDA 510(k)

THE HILL ADJUSTABLE HA90

K-Number: K931832 · 1993-06-29

ApplicantHill Laboratories Co.
Decision Date1993-06-29
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE HILL ADJUSTABLE HA90 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 1993-06-29 under 510(k) number K931832. 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 HA90?

THE HILL ADJUSTABLE HA90 is a medical device that received FDA 510(k) clearance on 1993-06-29. The listed applicant is Hill Laboratories Co.. The 510(k) number is K931832.

When did THE HILL ADJUSTABLE HA90 receive FDA 510(k) clearance?

THE HILL ADJUSTABLE HA90 received FDA 510(k) clearance on 1993-06-29, under 510(k) number K931832.

Who is the listed applicant for THE HILL ADJUSTABLE HA90?

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 HA90?

The FDA product code for THE HILL ADJUSTABLE HA90 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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