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FDA 510(k)

PROFESSONAL HI-LOW WORK TABLE MODEL 3400

K-Number: K932232 · 1993-07-22

Decision Date1993-07-22
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PROFESSONAL HI-LOW WORK TABLE MODEL 3400 is the device name listed in this FDA 510(k) record. The listed applicant is Bailey Mfg. Co.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K932232. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFESSONAL HI-LOW WORK TABLE MODEL 3400?

PROFESSONAL HI-LOW WORK TABLE MODEL 3400 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 K932232.

When did PROFESSONAL HI-LOW WORK TABLE MODEL 3400 receive FDA 510(k) clearance?

PROFESSONAL HI-LOW WORK TABLE MODEL 3400 received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932232.

Who is the listed applicant for PROFESSONAL HI-LOW WORK TABLE MODEL 3400?

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 PROFESSONAL HI-LOW WORK TABLE MODEL 3400?

The FDA product code for PROFESSONAL HI-LOW WORK TABLE MODEL 3400 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.

View all 11 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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