Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMERSON MOTION BED 6-MS & 6-ME

K-Number: K842604 · 1984-07-20

ApplicantJ. H. Emerson Co.
Decision Date1984-07-20
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMERSON MOTION BED 6-MS & 6-ME is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842604. 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 EMERSON MOTION BED 6-MS & 6-ME?

EMERSON MOTION BED 6-MS & 6-ME is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is J. H. Emerson Co.. The 510(k) number is K842604.

When did EMERSON MOTION BED 6-MS & 6-ME receive FDA 510(k) clearance?

EMERSON MOTION BED 6-MS & 6-ME received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842604.

Who is the listed applicant for EMERSON MOTION BED 6-MS & 6-ME?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERSON MOTION BED 6-MS & 6-ME?

The FDA product code for EMERSON MOTION BED 6-MS & 6-ME 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 J. H. Emerson 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.

K002598EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMINGK920910OXYGEN POWERED RESUSCITATOR FOR CPRK924174EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CAK902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMK896721MODEL 7-AT TREATMENT CHAMBERK881808EMERSON CHEST RESPIRATOR, MODEL 33-CRE

View all 25 devices →

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

View on FDA Database →

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

↑