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FDA 510(k)

LASERMED* GOGGLES AND SPECTACLES

K-Number: K894835 · 1989-09-21

ApplicantGlendale Protective Technologies, Inc.
Decision Date1989-09-21
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASERMED* GOGGLES AND SPECTACLES is the device name listed in this FDA 510(k) record. The listed applicant is Glendale Protective Technologies, Inc.. It received FDA 510(k) clearance on 1989-09-21 under 510(k) number K894835. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERMED* GOGGLES AND SPECTACLES?

LASERMED* GOGGLES AND SPECTACLES is a medical device that received FDA 510(k) clearance on 1989-09-21. The listed applicant is Glendale Protective Technologies, Inc.. The 510(k) number is K894835.

When did LASERMED* GOGGLES AND SPECTACLES receive FDA 510(k) clearance?

LASERMED* GOGGLES AND SPECTACLES received FDA 510(k) clearance on 1989-09-21, under 510(k) number K894835.

Who is the listed applicant for LASERMED* GOGGLES AND SPECTACLES?

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

What is the FDA product code for LASERMED* GOGGLES AND SPECTACLES?

The FDA product code for LASERMED* GOGGLES AND SPECTACLES is HQF.

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Other records listing Glendale Protective Technologies, 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.

K945920SUNGLASSES

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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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