POWER FLOSS AND BRUSH EW 129 & EW 120
K-Number: K914198 · 1991-12-18
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Device Summary
Frequently Asked Questions
What is the POWER FLOSS AND BRUSH EW 129 & EW 120?
POWER FLOSS AND BRUSH EW 129 & EW 120 is a medical device that received FDA 510(k) clearance on 1991-12-18. The listed applicant is Matsushita Electric Co.. The 510(k) number is K914198.
When did POWER FLOSS AND BRUSH EW 129 & EW 120 receive FDA 510(k) clearance?
POWER FLOSS AND BRUSH EW 129 & EW 120 received FDA 510(k) clearance on 1991-12-18, under 510(k) number K914198.
Who is the listed applicant for POWER FLOSS AND BRUSH EW 129 & EW 120?
The FDA 510(k) record lists Matsushita Electric Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWER FLOSS AND BRUSH EW 129 & EW 120?
The FDA product code for POWER FLOSS AND BRUSH EW 129 & EW 120 is JEQ.
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 Matsushita Electric Co. 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: JEQ)
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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