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FDA 510(k)

MARPAC MESSENGER MODEL #501

K-Number: K041485 · 2004-08-02

ApplicantMarpac, Inc.
Decision Date2004-08-02
Product CodeJOH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MARPAC MESSENGER MODEL #501 is the device name listed in this FDA 510(k) record. The listed applicant is Marpac, Inc.. It received FDA 510(k) clearance on 2004-08-02 under 510(k) number K041485. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARPAC MESSENGER MODEL #501?

MARPAC MESSENGER MODEL #501 is a medical device that received FDA 510(k) clearance on 2004-08-02. The listed applicant is Marpac, Inc.. The 510(k) number is K041485.

When did MARPAC MESSENGER MODEL #501 receive FDA 510(k) clearance?

MARPAC MESSENGER MODEL #501 received FDA 510(k) clearance on 2004-08-02, under 510(k) number K041485.

Who is the listed applicant for MARPAC MESSENGER MODEL #501?

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

What is the FDA product code for MARPAC MESSENGER MODEL #501?

The FDA product code for MARPAC MESSENGER MODEL #501 is JOH.

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Other records listing Marpac, Inc. as applicant

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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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