LARYNGOSCOPE RIGID
K-Number: K922019 · 1993-01-26
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Device Summary
Frequently Asked Questions
What is the LARYNGOSCOPE RIGID?
LARYNGOSCOPE RIGID is a medical device that received FDA 510(k) clearance on 1993-01-26. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K922019.
When did LARYNGOSCOPE RIGID receive FDA 510(k) clearance?
LARYNGOSCOPE RIGID received FDA 510(k) clearance on 1993-01-26, under 510(k) number K922019.
Who is the listed applicant for LARYNGOSCOPE RIGID?
The FDA 510(k) record lists Eastmed Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LARYNGOSCOPE RIGID?
The FDA product code for LARYNGOSCOPE RIGID is CCW.
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 Eastmed Enterprises, Inc. 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: CCW)
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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