ROBBETT MICROSURGICAL LARYNGOSCOPE
K-Number: K770085 · 1977-01-21
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Device Summary
Frequently Asked Questions
What is the ROBBETT MICROSURGICAL LARYNGOSCOPE?
ROBBETT MICROSURGICAL LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1977-01-21. The listed applicant is Edward Weck, Inc.. The 510(k) number is K770085.
When did ROBBETT MICROSURGICAL LARYNGOSCOPE receive FDA 510(k) clearance?
ROBBETT MICROSURGICAL LARYNGOSCOPE received FDA 510(k) clearance on 1977-01-21, under 510(k) number K770085.
Who is the listed applicant for ROBBETT MICROSURGICAL LARYNGOSCOPE?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROBBETT MICROSURGICAL LARYNGOSCOPE?
The FDA product code for ROBBETT MICROSURGICAL LARYNGOSCOPE is EQN.
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 Edward Weck, 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: EQN)
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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