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)

FDX SOLID STATE VIDEO CAMERA MODEL 5950

K-Number: K891236 · 1989-04-05

ApplicantMedical Dynamics, Inc.
Decision Date1989-04-05
Product CodeFWD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FDX SOLID STATE VIDEO CAMERA MODEL 5950 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dynamics, Inc.. It received FDA 510(k) clearance on 1989-04-05 under 510(k) number K891236. The device is classified under product code FWD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FDX SOLID STATE VIDEO CAMERA MODEL 5950?

FDX SOLID STATE VIDEO CAMERA MODEL 5950 is a medical device that received FDA 510(k) clearance on 1989-04-05. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K891236.

When did FDX SOLID STATE VIDEO CAMERA MODEL 5950 receive FDA 510(k) clearance?

FDX SOLID STATE VIDEO CAMERA MODEL 5950 received FDA 510(k) clearance on 1989-04-05, under 510(k) number K891236.

Who is the listed applicant for FDX SOLID STATE VIDEO CAMERA MODEL 5950?

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

What is the FDA product code for FDX SOLID STATE VIDEO CAMERA MODEL 5950?

The FDA product code for FDX SOLID STATE VIDEO CAMERA MODEL 5950 is FWD.

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 Dynamics, 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.

K974542TRUE VISION, TRUE VISION IIK921294VIDEO ENDOSCOPE-RIGID MODIFICATIONK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK930568ADAIR/VERESS NEEDLE INTRODUCER SETK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATION

View all 18 devices →

Related Devices (Code: FWD)

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.

K882166JEDMED MICRO CCD CAMERA SYSTEMJedmed Instrument Co.K862664JEDMED CCD CAMERA SYSTEMJedmed Instrument Co.K862145JEDMED MINI-MOS VIDEO CAMERAJedmed Instrument Co.K862034JEDMED CCD-02 VIDEO CAMERA SYSTEMJedmed Instrument Co.

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.

↑