ZENITH COX FLEXION CHIROPRACTIC TABLE
K-Number: K905685 · 1991-01-18
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Device Summary
Frequently Asked Questions
What is the ZENITH COX FLEXION CHIROPRACTIC TABLE?
ZENITH COX FLEXION CHIROPRACTIC TABLE is a medical device that received FDA 510(k) clearance on 1991-01-18. The listed applicant is Williams Manufacturing Co.. The 510(k) number is K905685.
When did ZENITH COX FLEXION CHIROPRACTIC TABLE receive FDA 510(k) clearance?
ZENITH COX FLEXION CHIROPRACTIC TABLE received FDA 510(k) clearance on 1991-01-18, under 510(k) number K905685.
Who is the listed applicant for ZENITH COX FLEXION 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 COX FLEXION CHIROPRACTIC TABLE?
The FDA product code for ZENITH COX FLEXION CHIROPRACTIC 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 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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