RHINO-LARYNX STROBOSCOPE TYPE 4914
K-Number: K842090 · 1984-07-18
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Device Summary
Frequently Asked Questions
What is the RHINO-LARYNX STROBOSCOPE TYPE 4914?
RHINO-LARYNX STROBOSCOPE TYPE 4914 is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Bruel & Kjaer Industri A/S. The 510(k) number is K842090.
When did RHINO-LARYNX STROBOSCOPE TYPE 4914 receive FDA 510(k) clearance?
RHINO-LARYNX STROBOSCOPE TYPE 4914 received FDA 510(k) clearance on 1984-07-18, under 510(k) number K842090.
Who is the listed applicant for RHINO-LARYNX STROBOSCOPE TYPE 4914?
The FDA 510(k) record lists Bruel & Kjaer Industri A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RHINO-LARYNX STROBOSCOPE TYPE 4914?
The FDA product code for RHINO-LARYNX STROBOSCOPE TYPE 4914 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 Bruel & Kjaer Industri A/S 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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