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)

ENDOSTROBOSCOPE IV

K-Number: K884933 · 1989-02-15

Decision Date1989-02-15
Product CodeEQL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDOSTROBOSCOPE IV is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1989-02-15 under 510(k) number K884933. The device is classified under product code EQL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSTROBOSCOPE IV?

ENDOSTROBOSCOPE IV is a medical device that received FDA 510(k) clearance on 1989-02-15. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K884933.

When did ENDOSTROBOSCOPE IV receive FDA 510(k) clearance?

ENDOSTROBOSCOPE IV received FDA 510(k) clearance on 1989-02-15, under 510(k) number K884933.

Who is the listed applicant for ENDOSTROBOSCOPE IV?

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

What is the FDA product code for ENDOSTROBOSCOPE IV?

The FDA product code for ENDOSTROBOSCOPE IV is EQL.

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 Jedmed Instrument 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.

View all 91 devices →

Related Devices (Code: EQL)

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.

↑