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FDA 510(k)

SLEEP MANAGEMENT SYSTEM

K-Number: K981844 · 1998-08-07

ApplicantRmp, Inc.
Decision Date1998-08-07
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SLEEP MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rmp, Inc.. It received FDA 510(k) clearance on 1998-08-07 under 510(k) number K981844. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLEEP MANAGEMENT SYSTEM?

SLEEP MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1998-08-07. The listed applicant is Rmp, Inc.. The 510(k) number is K981844.

When did SLEEP MANAGEMENT SYSTEM receive FDA 510(k) clearance?

SLEEP MANAGEMENT SYSTEM received FDA 510(k) clearance on 1998-08-07, under 510(k) number K981844.

Who is the listed applicant for SLEEP MANAGEMENT SYSTEM?

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

What is the FDA product code for SLEEP MANAGEMENT SYSTEM?

The FDA product code for SLEEP MANAGEMENT SYSTEM is HCC.

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Related Devices (Code: HCC)

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.

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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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