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FDA 510(k)

CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021

K-Number: K873983 · 1987-12-02

Decision Date1987-12-02
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021 is the device name listed in this FDA 510(k) record. The listed applicant is Arcotoys, Inc.. It received FDA 510(k) clearance on 1987-12-02 under 510(k) number K873983. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021?

CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021 is a medical device that received FDA 510(k) clearance on 1987-12-02. The listed applicant is Arcotoys, Inc.. The 510(k) number is K873983.

When did CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021 receive FDA 510(k) clearance?

CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021 received FDA 510(k) clearance on 1987-12-02, under 510(k) number K873983.

Who is the listed applicant for CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021?

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

What is the FDA product code for CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021?

The FDA product code for CAPTAIN POWER SUNGLASSES STYLES: #1020 #1021 is HQY.

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 Arcotoys, 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: HQY)

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

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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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