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)

UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT

K-Number: K853800 · 1985-10-07

ApplicantCedar Surgical, Inc.
Decision Date1985-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT is the device name listed in this FDA 510(k) record. The listed applicant is Cedar Surgical, Inc.. It received FDA 510(k) clearance on 1985-10-07 under 510(k) number K853800. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT?

UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT is a medical device that received FDA 510(k) clearance on 1985-10-07. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K853800.

When did UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT receive FDA 510(k) clearance?

UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT received FDA 510(k) clearance on 1985-10-07, under 510(k) number K853800.

Who is the listed applicant for UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT?

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

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 Cedar Surgical, 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.

K873692RAYLOR(TM) DRILL STOPK872281RAYLOR FUSION FUNNELK873690CEDAR(TM) PELVIC CUSHIONK873691CEDAR(TM) RETRACTOR RINGK864425RAYLOR(TM) DISSECTING HOOKK864421RAYLOR(TM) PERIOSTEAL ELEVATORS

View all 17 devices →

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.

↑