ELECTRIC TILT TABLE MODEL 9505
K-Number: K932239 · 1993-07-22
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Device Summary
Frequently Asked Questions
What is the ELECTRIC TILT TABLE MODEL 9505?
ELECTRIC TILT TABLE MODEL 9505 is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Bailey Mfg. Co.. The 510(k) number is K932239.
When did ELECTRIC TILT TABLE MODEL 9505 receive FDA 510(k) clearance?
ELECTRIC TILT TABLE MODEL 9505 received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932239.
Who is the listed applicant for ELECTRIC TILT TABLE MODEL 9505?
The FDA 510(k) record lists Bailey Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRIC TILT TABLE MODEL 9505?
The FDA product code for ELECTRIC TILT TABLE MODEL 9505 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 Bailey Mfg. 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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