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FDA 510(k)

MASSAGE MATTRESS VM9100RM

K-Number: K070672 · 2007-06-26

ApplicantMetek GmbH
Decision Date2007-06-26
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MASSAGE MATTRESS VM9100RM is the device name listed in this FDA 510(k) record. The listed applicant is Metek GmbH. It received FDA 510(k) clearance on 2007-06-26 under 510(k) number K070672. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASSAGE MATTRESS VM9100RM?

MASSAGE MATTRESS VM9100RM is a medical device that received FDA 510(k) clearance on 2007-06-26. The listed applicant is Metek GmbH. The 510(k) number is K070672.

When did MASSAGE MATTRESS VM9100RM receive FDA 510(k) clearance?

MASSAGE MATTRESS VM9100RM received FDA 510(k) clearance on 2007-06-26, under 510(k) number K070672.

Who is the listed applicant for MASSAGE MATTRESS VM9100RM?

The FDA 510(k) record lists Metek GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASSAGE MATTRESS VM9100RM?

The FDA product code for MASSAGE MATTRESS VM9100RM is JFB.

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Related Devices (Code: JFB)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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