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FDA 510(k)

SOLAZ

K-Number: K921685 · 1992-09-02

ApplicantSolarchromic, Inc.
Decision Date1992-09-02
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLAZ is the device name listed in this FDA 510(k) record. The listed applicant is Solarchromic, Inc.. It received FDA 510(k) clearance on 1992-09-02 under 510(k) number K921685. 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 SOLAZ?

SOLAZ is a medical device that received FDA 510(k) clearance on 1992-09-02. The listed applicant is Solarchromic, Inc.. The 510(k) number is K921685.

When did SOLAZ receive FDA 510(k) clearance?

SOLAZ received FDA 510(k) clearance on 1992-09-02, under 510(k) number K921685.

Who is the listed applicant for SOLAZ?

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

What is the FDA product code for SOLAZ?

The FDA product code for SOLAZ is HQY.

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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.

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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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