JEROME GLASS RING
K-Number: K023959 · 2003-02-21
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Device Summary
Frequently Asked Questions
What is the JEROME GLASS RING?
JEROME GLASS RING is a medical device that received FDA 510(k) clearance on 2003-02-21. The listed applicant is The Jerome Group, Inc.. The 510(k) number is K023959.
When did JEROME GLASS RING receive FDA 510(k) clearance?
JEROME GLASS RING received FDA 510(k) clearance on 2003-02-21, under 510(k) number K023959.
Who is the listed applicant for JEROME GLASS RING?
The FDA 510(k) record lists The Jerome Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JEROME GLASS RING?
The FDA product code for JEROME GLASS RING is HAX.
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 The Jerome Group, Inc. 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: HAX)
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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