MINI VIBRATOR
K-Number: K920487 · 1992-02-18
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Device Summary
Frequently Asked Questions
What is the MINI VIBRATOR?
MINI VIBRATOR is a medical device that received FDA 510(k) clearance on 1992-02-18. The listed applicant is Alimed, Inc.. The 510(k) number is K920487.
When did MINI VIBRATOR receive FDA 510(k) clearance?
MINI VIBRATOR received FDA 510(k) clearance on 1992-02-18, under 510(k) number K920487.
Who is the listed applicant for MINI VIBRATOR?
The FDA 510(k) record lists Alimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINI VIBRATOR?
The FDA product code for MINI VIBRATOR is IRO.
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 Alimed, 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: IRO)
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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