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FDA 510(k)

MULTIPLE LENS, SPECTACLES, CUSTOM

K-Number: K842187 · 1984-12-11

ApplicantPavuna , Ltd.
Decision Date1984-12-11
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULTIPLE LENS, SPECTACLES, CUSTOM is the device name listed in this FDA 510(k) record. The listed applicant is Pavuna , Ltd.. It received FDA 510(k) clearance on 1984-12-11 under 510(k) number K842187. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE LENS, SPECTACLES, CUSTOM?

MULTIPLE LENS, SPECTACLES, CUSTOM is a medical device that received FDA 510(k) clearance on 1984-12-11. The listed applicant is Pavuna , Ltd.. The 510(k) number is K842187.

When did MULTIPLE LENS, SPECTACLES, CUSTOM receive FDA 510(k) clearance?

MULTIPLE LENS, SPECTACLES, CUSTOM received FDA 510(k) clearance on 1984-12-11, under 510(k) number K842187.

Who is the listed applicant for MULTIPLE LENS, SPECTACLES, CUSTOM?

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

What is the FDA product code for MULTIPLE LENS, SPECTACLES, CUSTOM?

The FDA product code for MULTIPLE LENS, SPECTACLES, CUSTOM is HQG.

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.

Related Devices (Code: HQG)

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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