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FDA 510(k)

GlassBone Granules

K-Number: K242782 · 2024-12-23

ApplicantNoraker
Decision Date2024-12-23
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GlassBone Granules is the device name listed in this FDA 510(k) record. The listed applicant is Noraker. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K242782. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GlassBone Granules?

GlassBone Granules is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Noraker. The 510(k) number is K242782.

When did GlassBone Granules receive FDA 510(k) clearance?

GlassBone Granules received FDA 510(k) clearance on 2024-12-23, under 510(k) number K242782.

Who is the listed applicant for GlassBone Granules?

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

What is the FDA product code for GlassBone Granules?

The FDA product code for GlassBone Granules is MQV.

Related Devices (Code: MQV)

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

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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