AO STYLET LARYNGOSCOPE, MODEL SLS-1
K-Number: K791634 · 1979-09-17
Advertisement
Device Summary
Frequently Asked Questions
What is the AO STYLET LARYNGOSCOPE, MODEL SLS-1?
AO STYLET LARYNGOSCOPE, MODEL SLS-1 is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is American Optical Corp.. The 510(k) number is K791634.
When did AO STYLET LARYNGOSCOPE, MODEL SLS-1 receive FDA 510(k) clearance?
AO STYLET LARYNGOSCOPE, MODEL SLS-1 received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791634.
Who is the listed applicant for AO STYLET LARYNGOSCOPE, MODEL SLS-1?
The FDA 510(k) record lists American Optical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AO STYLET LARYNGOSCOPE, MODEL SLS-1?
The FDA product code for AO STYLET LARYNGOSCOPE, MODEL SLS-1 is CAL.
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 American Optical Corp. 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: CAL)
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.
Advertisement