VITALON CHAIR MASSAGER MODEL V-CHR2
K-Number: K890643 · 1989-02-22
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Device Summary
Frequently Asked Questions
What is the VITALON CHAIR MASSAGER MODEL V-CHR2?
VITALON CHAIR MASSAGER MODEL V-CHR2 is a medical device that received FDA 510(k) clearance on 1989-02-22. The listed applicant is Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd.. The 510(k) number is K890643.
When did VITALON CHAIR MASSAGER MODEL V-CHR2 receive FDA 510(k) clearance?
VITALON CHAIR MASSAGER MODEL V-CHR2 received FDA 510(k) clearance on 1989-02-22, under 510(k) number K890643.
Who is the listed applicant for VITALON CHAIR MASSAGER MODEL V-CHR2?
The FDA 510(k) record lists Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITALON CHAIR MASSAGER MODEL V-CHR2?
The FDA product code for VITALON CHAIR MASSAGER MODEL V-CHR2 is ISA.
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 Nexus Co. , Ltd. C/O Yama Trans Co. , Ltd. 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: ISA)
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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