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FDA 510(k)

EAR STOPPLES FOR NOISE ATTENTION

K-Number: K781907 · 1978-11-22

Decision Date1978-11-22
Product CodeEWD
DecisionSubstantially Equivalent

Device Summary

EAR STOPPLES FOR NOISE ATTENTION is the device name listed in this FDA 510(k) record. The listed applicant is Crown Delta Corp.. It received FDA 510(k) clearance on 1978-11-22 under 510(k) number K781907. The device is classified under product code EWD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAR STOPPLES FOR NOISE ATTENTION?

EAR STOPPLES FOR NOISE ATTENTION is a medical device that received FDA 510(k) clearance on 1978-11-22. The listed applicant is Crown Delta Corp.. The 510(k) number is K781907.

When did EAR STOPPLES FOR NOISE ATTENTION receive FDA 510(k) clearance?

EAR STOPPLES FOR NOISE ATTENTION received FDA 510(k) clearance on 1978-11-22, under 510(k) number K781907.

Who is the listed applicant for EAR STOPPLES FOR NOISE ATTENTION?

The FDA 510(k) record lists Crown Delta Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EAR STOPPLES FOR NOISE ATTENTION?

The FDA product code for EAR STOPPLES FOR NOISE ATTENTION is EWD.

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 Crown Delta Corp. 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 18 devices →

Related Devices (Code: EWD)

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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