Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

THE HILL ADJUSTABLE RATH MECHANICAL TABLE

K-Number: K942109 · 1995-06-22

Decision Date1995-06-22
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE HILL ADJUSTABLE RATH MECHANICAL TABLE 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 K942109. 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 RATH MECHANICAL TABLE?

THE HILL ADJUSTABLE RATH MECHANICAL TABLE 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 K942109.

When did THE HILL ADJUSTABLE RATH MECHANICAL TABLE receive FDA 510(k) clearance?

THE HILL ADJUSTABLE RATH MECHANICAL TABLE received FDA 510(k) clearance on 1995-06-22, under 510(k) number K942109.

Who is the listed applicant for THE HILL ADJUSTABLE RATH MECHANICAL TABLE?

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 RATH MECHANICAL TABLE?

The FDA product code for THE HILL ADJUSTABLE RATH MECHANICAL TABLE is INQ.

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.

Other records listing Hill Laboratories Co. as applicant

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.

View all 17 devices →

Related Devices (Code: INQ)

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

View on FDA Database →

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

↑