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FDA 510(k)

A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH

K-Number: K872525 · 1988-02-22

ApplicantM.C. Johnson Co., Inc.
Decision Date1988-02-22
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH is the device name listed in this FDA 510(k) record. The listed applicant is M.C. Johnson Co., Inc.. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K872525. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH?

A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is M.C. Johnson Co., Inc.. The 510(k) number is K872525.

When did A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH receive FDA 510(k) clearance?

A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH received FDA 510(k) clearance on 1988-02-22, under 510(k) number K872525.

Who is the listed applicant for A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH?

The FDA 510(k) record lists M.C. Johnson Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH?

The FDA product code for A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH is KPR.

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 M.C. Johnson Co., Inc. 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.

K953375NG SECUREK832702POCKET AID

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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