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FDA 510(k)

PRO. HI-LOW MAT TABLES #9610-9612 9620-9622

K-Number: K932235 · 1993-07-22

ApplicantBailey Mfg. Co.
Decision Date1993-07-22
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 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 K932235. 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 PRO. HI-LOW MAT TABLES #9610-9612 9620-9622?

PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 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 K932235.

When did PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 receive FDA 510(k) clearance?

PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932235.

Who is the listed applicant for PRO. HI-LOW MAT TABLES #9610-9612 9620-9622?

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 PRO. HI-LOW MAT TABLES #9610-9612 9620-9622?

The FDA product code for PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 is INQ.

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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.

K932240MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARSK932241ECONOMY HI-LOW MAT TABLES/ELECTRIC MODELSK932231ECONOMY HI-LOW MAT TABLE #4110 THRU 4117K932233ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405K932238ECO. HI-LOW TREATMENT TABLES VARIOUS MODEL NUMBERSK932236PRO. HI-LOW TABLE MODEL 9530

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

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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