FIBER OPTIC HEADLIGHT #60-0766766
K-Number: K802770 · 1980-12-11
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Device Summary
Frequently Asked Questions
What is the FIBER OPTIC HEADLIGHT #60-0766766?
FIBER OPTIC HEADLIGHT #60-0766766 is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K802770.
When did FIBER OPTIC HEADLIGHT #60-0766766 receive FDA 510(k) clearance?
FIBER OPTIC HEADLIGHT #60-0766766 received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802770.
Who is the listed applicant for FIBER OPTIC HEADLIGHT #60-0766766?
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 HEADLIGHT #60-0766766?
The FDA product code for FIBER OPTIC HEADLIGHT #60-0766766 is FCT.
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: FCT)
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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