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FDA 510(k)

SOLAR SPECS

K-Number: K970759 · 1997-05-06

ApplicantMorris Rosenbloom & Co., Inc.
Decision Date1997-05-06
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLAR SPECS is the device name listed in this FDA 510(k) record. The listed applicant is Morris Rosenbloom & Co., Inc.. It received FDA 510(k) clearance on 1997-05-06 under 510(k) number K970759. 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 SOLAR SPECS?

SOLAR SPECS is a medical device that received FDA 510(k) clearance on 1997-05-06. The listed applicant is Morris Rosenbloom & Co., Inc.. The 510(k) number is K970759.

When did SOLAR SPECS receive FDA 510(k) clearance?

SOLAR SPECS received FDA 510(k) clearance on 1997-05-06, under 510(k) number K970759.

Who is the listed applicant for SOLAR SPECS?

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

What is the FDA product code for SOLAR SPECS?

The FDA product code for SOLAR SPECS 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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