ENDOSTROBOSCOPE IV
K-Number: K884933 · 1989-02-15
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Device Summary
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.
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.
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