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)

VKG 1000, VIDEO KERATOGRAPH

K-Number: K901523 · 1990-06-27

ApplicantThe Sanborn Co.
Decision Date1990-06-27
Product CodeHJA
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VKG 1000, VIDEO KERATOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is The Sanborn Co.. It received FDA 510(k) clearance on 1990-06-27 under 510(k) number K901523. The device is classified under product code HJA. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VKG 1000, VIDEO KERATOGRAPH?

VKG 1000, VIDEO KERATOGRAPH is a medical device that received FDA 510(k) clearance on 1990-06-27. The listed applicant is The Sanborn Co.. The 510(k) number is K901523.

When did VKG 1000, VIDEO KERATOGRAPH receive FDA 510(k) clearance?

VKG 1000, VIDEO KERATOGRAPH received FDA 510(k) clearance on 1990-06-27, under 510(k) number K901523.

Who is the listed applicant for VKG 1000, VIDEO KERATOGRAPH?

The FDA 510(k) record lists The Sanborn Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VKG 1000, VIDEO KERATOGRAPH?

The FDA product code for VKG 1000, VIDEO KERATOGRAPH is HJA.

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 The Sanborn Co. 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.

K901553SURG-K SURGICAL KERATOMETER

Related Devices (Code: HJA)

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.

K893968VKG 2000 VIDEO KERATOMETERTechnitex, Inc.K842128AMERICAN MEDICAL OPTICS PHOTOKERATOAmerican Medical OpticsK830290DORC CONTACT/PHOTO DERATOSCOPEJedmed Instrument Co.K781650TERRY KERATOMETERClifford M. Terry, M.C.

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.

↑