FIBER OPTIC LIGHT GUIDE CAT#60-0768
K-Number: K802767 · 1980-12-16
Advertisement
Device Summary
Frequently Asked Questions
What is the FIBER OPTIC LIGHT GUIDE CAT#60-0768?
FIBER OPTIC LIGHT GUIDE CAT#60-0768 is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K802767.
When did FIBER OPTIC LIGHT GUIDE CAT#60-0768 receive FDA 510(k) clearance?
FIBER OPTIC LIGHT GUIDE CAT#60-0768 received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802767.
Who is the listed applicant for FIBER OPTIC LIGHT GUIDE CAT#60-0768?
The FDA 510(k) record lists Aspen Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIBER OPTIC LIGHT GUIDE CAT#60-0768?
The FDA product code for FIBER OPTIC LIGHT GUIDE CAT#60-0768 is EQH.
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 Aspen Laboratories, 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: EQH)
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