INFRAVIB MASSAGER - MODEL PR-1000
K-Number: K900384 · 1990-02-27
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Device Summary
Frequently Asked Questions
What is the INFRAVIB MASSAGER - MODEL PR-1000?
INFRAVIB MASSAGER - MODEL PR-1000 is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Infralux International, Inc.. The 510(k) number is K900384.
When did INFRAVIB MASSAGER - MODEL PR-1000 receive FDA 510(k) clearance?
INFRAVIB MASSAGER - MODEL PR-1000 received FDA 510(k) clearance on 1990-02-27, under 510(k) number K900384.
Who is the listed applicant for INFRAVIB MASSAGER - MODEL PR-1000?
The FDA 510(k) record lists Infralux International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFRAVIB MASSAGER - MODEL PR-1000?
The FDA product code for INFRAVIB MASSAGER - MODEL PR-1000 is ILY.
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 Infralux International, 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: ILY)
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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