ZENITH TRAVELER CHIROPRACTIC TABLE
K-Number: K880222 · 1988-02-03
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Device Summary
Frequently Asked Questions
What is the ZENITH TRAVELER CHIROPRACTIC TABLE?
ZENITH TRAVELER CHIROPRACTIC TABLE is a medical device that received FDA 510(k) clearance on 1988-02-03. The listed applicant is Williams Manufacturing Co.. The 510(k) number is K880222.
When did ZENITH TRAVELER CHIROPRACTIC TABLE receive FDA 510(k) clearance?
ZENITH TRAVELER CHIROPRACTIC TABLE received FDA 510(k) clearance on 1988-02-03, under 510(k) number K880222.
Who is the listed applicant for ZENITH TRAVELER CHIROPRACTIC TABLE?
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 TRAVELER CHIROPRACTIC TABLE?
The FDA product code for ZENITH TRAVELER CHIROPRACTIC TABLE is INW.
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: INW)
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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