CONPHAR LARYNGOSCOPE
K-Number: K813297 · 1982-01-22
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Device Summary
Frequently Asked Questions
What is the CONPHAR LARYNGOSCOPE?
CONPHAR LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Conphar, Inc.. The 510(k) number is K813297.
When did CONPHAR LARYNGOSCOPE receive FDA 510(k) clearance?
CONPHAR LARYNGOSCOPE received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813297.
Who is the listed applicant for CONPHAR LARYNGOSCOPE?
The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONPHAR LARYNGOSCOPE?
The FDA product code for CONPHAR 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 Conphar, 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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