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)

LIGHT COMMANDER

K-Number: K960767 · 1996-08-26

ApplicantScieran Technologies, Inc.
Decision Date1996-08-26
Product CodeFCT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LIGHT COMMANDER is the device name listed in this FDA 510(k) record. The listed applicant is Scieran Technologies, Inc.. It received FDA 510(k) clearance on 1996-08-26 under 510(k) number K960767. The device is classified under product code FCT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT COMMANDER?

LIGHT COMMANDER is a medical device that received FDA 510(k) clearance on 1996-08-26. The listed applicant is Scieran Technologies, Inc.. The 510(k) number is K960767.

When did LIGHT COMMANDER receive FDA 510(k) clearance?

LIGHT COMMANDER received FDA 510(k) clearance on 1996-08-26, under 510(k) number K960767.

Who is the listed applicant for LIGHT COMMANDER?

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

What is the FDA product code for LIGHT COMMANDER?

The FDA product code for LIGHT COMMANDER is FCT.

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 Scieran Technologies, 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.

K974253CPD COMMANDERK980085PHACO COMMANDERK973749FRAG COMMANDERK961738VIT COMMANDER SYSTEM

Related Devices (Code: FCT)

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.

K924198MODIFIED SITE FIBER OPTIC MODULEChiron Vision Corp.K883480MODIFIED SITE FIBER OPTIC MODULE FOR OPHTHAL. USESite Microsurgical Systems, Inc.K802769FIBER OPTIC HEADLIGHT #60-0765Aspen Laboratories, Inc.K802770FIBER OPTIC HEADLIGHT #60-0766766Aspen Laboratories, Inc.K780433FIBER OPTIC ADJUSTABLE HEADLIGHTCameron-Miller, 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.

↑