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FDA 510(k)

Crown HT

K-Number: K242277 · 2024-10-01

Decision Date2024-10-01
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Crown HT is the device name listed in this FDA 510(k) record. The listed applicant is Sprintray, Inc.. It received FDA 510(k) clearance on 2024-10-01 under 510(k) number K242277. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Crown HT?

Crown HT is a medical device that received FDA 510(k) clearance on 2024-10-01. The listed applicant is Sprintray, Inc.. The 510(k) number is K242277.

When did Crown HT receive FDA 510(k) clearance?

Crown HT received FDA 510(k) clearance on 2024-10-01, under 510(k) number K242277.

Who is the listed applicant for Crown HT?

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

What is the FDA product code for Crown HT?

The FDA product code for Crown HT is EBF.

Other records listing Sprintray, 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.

View all 9 devices →

Related Devices (Code: EBF)

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.