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)

MEDICAL DISPOSABLE BEDDING

K-Number: K924420 · 1993-12-10

ApplicantHill-Rom, Inc.
Decision Date1993-12-10
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDICAL DISPOSABLE BEDDING is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom, Inc.. It received FDA 510(k) clearance on 1993-12-10 under 510(k) number K924420. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL DISPOSABLE BEDDING?

MEDICAL DISPOSABLE BEDDING is a medical device that received FDA 510(k) clearance on 1993-12-10. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K924420.

When did MEDICAL DISPOSABLE BEDDING receive FDA 510(k) clearance?

MEDICAL DISPOSABLE BEDDING received FDA 510(k) clearance on 1993-12-10, under 510(k) number K924420.

Who is the listed applicant for MEDICAL DISPOSABLE BEDDING?

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

What is the FDA product code for MEDICAL DISPOSABLE BEDDING?

The FDA product code for MEDICAL DISPOSABLE BEDDING is KNC.

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 Hill-Rom, 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.

K260211Dashboard (P007000)K202018Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor ActivationK180079Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor ActivationK013709HILL-ROM PRIMAVIEW MONITOR SYSTEMK973705CONTOR TABLE SURFACEK981081BRIGHTSTAR

View all 34 devices →

Related Devices (Code: KNC)

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.

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SAK932035NON-LINTING DELIVERY BLANKETAmsco Sterile Recoveries, Inc.K914544BD6000 THE OPTIMA & BD5000 BIRTHING BEDLic Care, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls Corp.K884868OBSTETRICAL SAFETY SYSTEMBuckman Co., 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.

↑