Decision Date2022-02-17
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Amazing+ is the device name listed in this FDA 510(k) record. The listed applicant is Amazing Rubber Products Pvt, Ltd.. It received FDA 510(k) clearance on 2022-02-17 under 510(k) number K212586. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Amazing+?
Amazing+ is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Amazing Rubber Products Pvt, Ltd.. The 510(k) number is K212586.
When did Amazing+ receive FDA 510(k) clearance?
Amazing+ received FDA 510(k) clearance on 2022-02-17, under 510(k) number K212586.
Who is the listed applicant for Amazing+?
The FDA 510(k) record lists Amazing Rubber Products Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Amazing+?
The FDA product code for Amazing+ is LZA.
Related Clinical Trials
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Other records listing Amazing Rubber Products Pvt, Ltd. 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.
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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.