BRIMFIELD FIBEROPTIC LIGHT SCOURCE
K-Number: K841731 · 1984-07-16
Advertisement
Device Summary
Frequently Asked Questions
What is the BRIMFIELD FIBEROPTIC LIGHT SCOURCE?
BRIMFIELD FIBEROPTIC LIGHT SCOURCE is a medical device that received FDA 510(k) clearance on 1984-07-16. The listed applicant is Brimfield Scientific Instruments. The 510(k) number is K841731.
When did BRIMFIELD FIBEROPTIC LIGHT SCOURCE receive FDA 510(k) clearance?
BRIMFIELD FIBEROPTIC LIGHT SCOURCE received FDA 510(k) clearance on 1984-07-16, under 510(k) number K841731.
Who is the listed applicant for BRIMFIELD FIBEROPTIC LIGHT SCOURCE?
The FDA 510(k) record lists Brimfield Scientific Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRIMFIELD FIBEROPTIC LIGHT SCOURCE?
The FDA product code for BRIMFIELD FIBEROPTIC LIGHT SCOURCE 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 Brimfield Scientific Instruments 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