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FDA 510(k)

KEANE MOBILITY BED

K-Number: K873047 · 1987-10-15

ApplicantSurgi-Med, Inc.
Decision Date1987-10-15
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KEANE MOBILITY BED is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Med, Inc.. It received FDA 510(k) clearance on 1987-10-15 under 510(k) number K873047. The device is classified under product code IKZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEANE MOBILITY BED?

KEANE MOBILITY BED is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Surgi-Med, Inc.. The 510(k) number is K873047.

When did KEANE MOBILITY BED receive FDA 510(k) clearance?

KEANE MOBILITY BED received FDA 510(k) clearance on 1987-10-15, under 510(k) number K873047.

Who is the listed applicant for KEANE MOBILITY BED?

The FDA 510(k) record lists Surgi-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KEANE MOBILITY BED?

The FDA product code for KEANE MOBILITY BED is IKZ.

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 Surgi-Med, 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.

K881705MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEMK872923PARAGON 9000 TILT AND TURN BEDK872924PARAGON 8500 CARDIO-PULMONARY BEDK872925MEGABED 1000

Related Devices (Code: IKZ)

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.

K972486PRESSUREGUARD IVSpan-America Medical Systems, Inc.K972111RUMORS DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K962788CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMGaymar Industries, Inc.K954671THE FREEDOM BEDProbed Medical Technologies, Inc.K950756PULMONEX DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K950681MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPYInvacare Corp.

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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