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)

STRETCHER TABLE

K-Number: K884292 · 1989-03-31

ApplicantFischer Imaging Corp.
Decision Date1989-03-31
Product CodeKXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STRETCHER TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1989-03-31 under 510(k) number K884292. The device is classified under product code KXH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRETCHER TABLE?

STRETCHER TABLE is a medical device that received FDA 510(k) clearance on 1989-03-31. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K884292.

When did STRETCHER TABLE receive FDA 510(k) clearance?

STRETCHER TABLE received FDA 510(k) clearance on 1989-03-31, under 510(k) number K884292.

Who is the listed applicant for STRETCHER TABLE?

The FDA 510(k) record lists Fischer Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRETCHER TABLE?

The FDA product code for STRETCHER TABLE is KXH.

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 Fischer Imaging Corp. 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.

K042095MAMMOTESTK021113MAMMOPATHK981414LC POSITIONERK973400MAMMOTEST ADAPTER DRIVERK964806MD-1835K961207EP-X BIPLANE

View all 69 devices →

Related Devices (Code: KXH)

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.

K122174PEDIATRIC POSITIONER PAD SETGe Healthcare Coils (Usa Instruments, Inc.)K953246OCTOROLLOctostop, Inc.K930124VARIANT OF OCTOSTOP AND OCTOPAQUEOctostop, Inc.K933134SPECTRUM DG-P7000 PEDIATRIC CRADLESpectrum X-Ray Corp.K930357ACCESSORY TO UNIVERSAL OCTOPAQUEOctostop, Inc.K863890MAMM-AIREAr Custom Medical Products, Ltd.

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.

↑