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)

RAYLOR(TM) PROTECTIVE RETRACTOR

K-Number: K864424 · 1986-11-26

ApplicantCedar Surgical, Inc.
Decision Date1986-11-26
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAYLOR(TM) PROTECTIVE RETRACTOR 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 1986-11-26 under 510(k) number K864424. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYLOR(TM) PROTECTIVE RETRACTOR?

RAYLOR(TM) PROTECTIVE RETRACTOR is a medical device that received FDA 510(k) clearance on 1986-11-26. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K864424.

When did RAYLOR(TM) PROTECTIVE RETRACTOR receive FDA 510(k) clearance?

RAYLOR(TM) PROTECTIVE RETRACTOR received FDA 510(k) clearance on 1986-11-26, under 510(k) number K864424.

Who is the listed applicant for RAYLOR(TM) PROTECTIVE RETRACTOR?

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

What is the FDA product code for RAYLOR(TM) PROTECTIVE RETRACTOR?

The FDA product code for RAYLOR(TM) PROTECTIVE RETRACTOR is GAD.

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 HOOKK864426RAYLOR(TM) DEPTH GAUGE

View all 17 devices →

Related Devices (Code: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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.

↑