ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES
K-Number: K902971 · 1990-07-26
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Device Summary
Frequently Asked Questions
What is the ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES?
ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Williams Manufacturing Co.. The 510(k) number is K902971.
When did ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES receive FDA 510(k) clearance?
ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES received FDA 510(k) clearance on 1990-07-26, under 510(k) number K902971.
Who is the listed applicant for ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES?
The FDA 510(k) record lists Williams Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES?
The FDA product code for ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES 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 Williams Manufacturing 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.
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