THE HILL HI-LO TABLE
K-Number: K934754 · 1995-02-17
Advertisement
Device Summary
Frequently Asked Questions
What is the THE HILL HI-LO TABLE?
THE HILL HI-LO TABLE is a medical device that received FDA 510(k) clearance on 1995-02-17. The listed applicant is Hill Laboratories Co.. The 510(k) number is K934754.
When did THE HILL HI-LO TABLE receive FDA 510(k) clearance?
THE HILL HI-LO TABLE received FDA 510(k) clearance on 1995-02-17, under 510(k) number K934754.
Who is the listed applicant for THE HILL HI-LO 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 HI-LO TABLE?
The FDA product code for THE HILL HI-LO 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.
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.
Advertisement