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)

ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE

K-Number: K905282 · 1991-03-19

Decision Date1991-03-19
Product CodeGCT
Advisory CommitteeGU
DecisionUnknown

Device Summary

ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Frantz Medical Development, Ltd.. It received FDA 510(k) clearance on 1991-03-19 under 510(k) number K905282. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE?

ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1991-03-19. The listed applicant is Frantz Medical Development, Ltd.. The 510(k) number is K905282.

When did ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE receive FDA 510(k) clearance?

ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE received FDA 510(k) clearance on 1991-03-19, under 510(k) number K905282.

Who is the listed applicant for ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE?

The FDA 510(k) record lists Frantz Medical Development, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE?

The FDA product code for ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE is GCT.

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 Frantz Medical Development, 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: GCT)

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.

↑