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FDA 510(k)

MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS

K-Number: K932240 · 1994-04-01

ApplicantBailey Mfg. Co.
Decision Date1994-04-01
Product CodeIRR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS 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 1994-04-01 under 510(k) number K932240. The device is classified under product code IRR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS?

MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Bailey Mfg. Co.. The 510(k) number is K932240.

When did MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS receive FDA 510(k) clearance?

MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS received FDA 510(k) clearance on 1994-04-01, under 510(k) number K932240.

Who is the listed applicant for MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS?

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 MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS?

The FDA product code for MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS is IRR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K932236PRO. HI-LOW TABLE MODEL 9530K932241ECONOMY 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 NUMBERSK932237PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090

View all 11 devices →

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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