LARYNGEAL MIRROR PRE-WARMER
K-Number: K855021 · 1986-03-20
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Device Summary
Frequently Asked Questions
What is the LARYNGEAL MIRROR PRE-WARMER?
LARYNGEAL MIRROR PRE-WARMER is a medical device that received FDA 510(k) clearance on 1986-03-20. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K855021.
When did LARYNGEAL MIRROR PRE-WARMER receive FDA 510(k) clearance?
LARYNGEAL MIRROR PRE-WARMER received FDA 510(k) clearance on 1986-03-20, under 510(k) number K855021.
Who is the listed applicant for LARYNGEAL MIRROR PRE-WARMER?
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 LARYNGEAL MIRROR PRE-WARMER?
The FDA product code for LARYNGEAL MIRROR PRE-WARMER is ETF.
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: ETF)
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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