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)

SONY COLOR VIDEO CAMERAS AND ACCESSORIES

K-Number: K884343 · 1988-11-01

ApplicantSony Corp. of America
Decision Date1988-11-01
Product CodeFWB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SONY COLOR VIDEO CAMERAS AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Sony Corp. of America. It received FDA 510(k) clearance on 1988-11-01 under 510(k) number K884343. The device is classified under product code FWB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY COLOR VIDEO CAMERAS AND ACCESSORIES?

SONY COLOR VIDEO CAMERAS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1988-11-01. The listed applicant is Sony Corp. of America. The 510(k) number is K884343.

When did SONY COLOR VIDEO CAMERAS AND ACCESSORIES receive FDA 510(k) clearance?

SONY COLOR VIDEO CAMERAS AND ACCESSORIES received FDA 510(k) clearance on 1988-11-01, under 510(k) number K884343.

Who is the listed applicant for SONY COLOR VIDEO CAMERAS AND ACCESSORIES?

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

What is the FDA product code for SONY COLOR VIDEO CAMERAS AND ACCESSORIES?

The FDA product code for SONY COLOR VIDEO CAMERAS AND ACCESSORIES is FWB.

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 Sony Corp. of America 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.

K890826SONY VIDEO GRAPHIC PRINTER UP-850

Related Devices (Code: FWB)

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.

K934092CAMERA, SURGICAL AND ACCESSORIESEnvision Medical Corp.K902359SURGICAL VIDEO CAMERA, MODEL 9500Seitz Technical Products, Inc.K871057MC-SERIES SURGICAL CAMERASM.P. Video, Inc.K855020MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930Medline Industries, Inc.K820829MEDICAMM.P. Video, 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.

↑