EYE SPONGE OR SPEAR
K-Number: K834356 · 1984-03-16
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Device Summary
Frequently Asked Questions
What is the EYE SPONGE OR SPEAR?
EYE SPONGE OR SPEAR is a medical device that received FDA 510(k) clearance on 1984-03-16. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K834356.
When did EYE SPONGE OR SPEAR receive FDA 510(k) clearance?
EYE SPONGE OR SPEAR received FDA 510(k) clearance on 1984-03-16, under 510(k) number K834356.
Who is the listed applicant for EYE SPONGE OR SPEAR?
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 EYE SPONGE OR SPEAR?
The FDA product code for EYE SPONGE OR SPEAR is HOZ.
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: HOZ)
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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