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)

DISPOSABLE VASCULAR ANGIOSCOPE

K-Number: K914570 · 1992-01-27

ApplicantNobles-Lai
Decision Date1992-01-27
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE VASCULAR ANGIOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Nobles-Lai. It received FDA 510(k) clearance on 1992-01-27 under 510(k) number K914570. The device is classified under product code LYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE VASCULAR ANGIOSCOPE?

DISPOSABLE VASCULAR ANGIOSCOPE is a medical device that received FDA 510(k) clearance on 1992-01-27. The listed applicant is Nobles-Lai. The 510(k) number is K914570.

When did DISPOSABLE VASCULAR ANGIOSCOPE receive FDA 510(k) clearance?

DISPOSABLE VASCULAR ANGIOSCOPE received FDA 510(k) clearance on 1992-01-27, under 510(k) number K914570.

Who is the listed applicant for DISPOSABLE VASCULAR ANGIOSCOPE?

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

What is the FDA product code for DISPOSABLE VASCULAR ANGIOSCOPE?

The FDA product code for DISPOSABLE VASCULAR ANGIOSCOPE is LYK.

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.

Related Devices (Code: LYK)

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.

↑