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FDA 510(k)

SWISS OPTICAL PRODUCTS-CONTACT CASE

K-Number: K840115 · 1984-06-01

Decision Date1984-06-01
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SWISS OPTICAL PRODUCTS-CONTACT CASE is the device name listed in this FDA 510(k) record. The listed applicant is Moonbeam International, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K840115. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWISS OPTICAL PRODUCTS-CONTACT CASE?

SWISS OPTICAL PRODUCTS-CONTACT CASE is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Moonbeam International, Inc.. The 510(k) number is K840115.

When did SWISS OPTICAL PRODUCTS-CONTACT CASE receive FDA 510(k) clearance?

SWISS OPTICAL PRODUCTS-CONTACT CASE received FDA 510(k) clearance on 1984-06-01, under 510(k) number K840115.

Who is the listed applicant for SWISS OPTICAL PRODUCTS-CONTACT CASE?

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

What is the FDA product code for SWISS OPTICAL PRODUCTS-CONTACT CASE?

The FDA product code for SWISS OPTICAL PRODUCTS-CONTACT CASE is HQD.

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 Moonbeam International, 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: HQD)

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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