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FDA 510(k)

Bevel Up Holder

K-Number: K193074 · 2020-04-21

ApplicantNsp Tech Pte, Ltd.
Decision Date2020-04-21
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Bevel Up Holder is the device name listed in this FDA 510(k) record. The listed applicant is Nsp Tech Pte, Ltd.. It received FDA 510(k) clearance on 2020-04-21 under 510(k) number K193074. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bevel Up Holder?

Bevel Up Holder is a medical device that received FDA 510(k) clearance on 2020-04-21. The listed applicant is Nsp Tech Pte, Ltd.. The 510(k) number is K193074.

When did Bevel Up Holder receive FDA 510(k) clearance?

Bevel Up Holder received FDA 510(k) clearance on 2020-04-21, under 510(k) number K193074.

Who is the listed applicant for Bevel Up Holder?

The FDA 510(k) record lists Nsp Tech Pte, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bevel Up Holder?

The FDA product code for Bevel Up Holder is JKA.

Other records listing Nsp Tech Pte, 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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Related Devices (Code: JKA)

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

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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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