STARband, STARlight, St. Louis Band
K-Number: K203098 · 2021-04-27
Device Summary
Frequently Asked Questions
What is the STARband, STARlight, St. Louis Band?
STARband, STARlight, St. Louis Band is a medical device that received FDA 510(k) clearance on 2021-04-27. The listed applicant is Orthomerica Products, Inc.. The 510(k) number is K203098.
When did STARband, STARlight, St. Louis Band receive FDA 510(k) clearance?
STARband, STARlight, St. Louis Band received FDA 510(k) clearance on 2021-04-27, under 510(k) number K203098.
Who is the listed applicant for STARband, STARlight, St. Louis Band?
The FDA 510(k) record lists Orthomerica Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STARband, STARlight, St. Louis Band?
The FDA product code for STARband, STARlight, St. Louis Band is OAN.
Other records listing Orthomerica Products, 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: OAN)
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.