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)

TILT TYPE AC POWERED HOSPITAL BED

K-Number: K780371 · 1978-04-10

ApplicantMedical Specialty Products, Inc.
Decision Date1978-04-10
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TILT TYPE AC POWERED HOSPITAL BED is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialty Products, Inc.. It received FDA 510(k) clearance on 1978-04-10 under 510(k) number K780371. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TILT TYPE AC POWERED HOSPITAL BED?

TILT TYPE AC POWERED HOSPITAL BED is a medical device that received FDA 510(k) clearance on 1978-04-10. The listed applicant is Medical Specialty Products, Inc.. The 510(k) number is K780371.

When did TILT TYPE AC POWERED HOSPITAL BED receive FDA 510(k) clearance?

TILT TYPE AC POWERED HOSPITAL BED received FDA 510(k) clearance on 1978-04-10, under 510(k) number K780371.

Who is the listed applicant for TILT TYPE AC POWERED HOSPITAL BED?

The FDA 510(k) record lists Medical Specialty Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TILT TYPE AC POWERED HOSPITAL BED?

The FDA product code for TILT TYPE AC POWERED HOSPITAL BED is FNL.

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 Medical Specialty Products, 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.

K780370STAND UP TOILET

Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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.

↑