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)

VISION-TECH YZ SLIT LAMP, MODEL 66

K-Number: K033190 · 2003-12-04

Decision Date2003-12-04
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISION-TECH YZ SLIT LAMP, MODEL 66 is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou 66 Vision-Tech Co., Ltd.. It received FDA 510(k) clearance on 2003-12-04 under 510(k) number K033190. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION-TECH YZ SLIT LAMP, MODEL 66?

VISION-TECH YZ SLIT LAMP, MODEL 66 is a medical device that received FDA 510(k) clearance on 2003-12-04. The listed applicant is Suzhou 66 Vision-Tech Co., Ltd.. The 510(k) number is K033190.

When did VISION-TECH YZ SLIT LAMP, MODEL 66 receive FDA 510(k) clearance?

VISION-TECH YZ SLIT LAMP, MODEL 66 received FDA 510(k) clearance on 2003-12-04, under 510(k) number K033190.

Who is the listed applicant for VISION-TECH YZ SLIT LAMP, MODEL 66?

The FDA 510(k) record lists Suzhou 66 Vision-Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISION-TECH YZ SLIT LAMP, MODEL 66?

The FDA product code for VISION-TECH YZ SLIT LAMP, MODEL 66 is HJO.

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.

Other records listing Suzhou 66 Vision-Tech Co., Ltd. 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.

Related Devices (Code: HJO)

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.

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.

↑