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FDA 510(k)

SUNSHADES, ACRYLIC LENSES, ORDER #SG-01

K-Number: K902385 · 1990-07-05

Decision Date1990-07-05
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNSHADES, ACRYLIC LENSES, ORDER #SG-01 is the device name listed in this FDA 510(k) record. The listed applicant is Tel-Time Products. It received FDA 510(k) clearance on 1990-07-05 under 510(k) number K902385. 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 SUNSHADES, ACRYLIC LENSES, ORDER #SG-01?

SUNSHADES, ACRYLIC LENSES, ORDER #SG-01 is a medical device that received FDA 510(k) clearance on 1990-07-05. The listed applicant is Tel-Time Products. The 510(k) number is K902385.

When did SUNSHADES, ACRYLIC LENSES, ORDER #SG-01 receive FDA 510(k) clearance?

SUNSHADES, ACRYLIC LENSES, ORDER #SG-01 received FDA 510(k) clearance on 1990-07-05, under 510(k) number K902385.

Who is the listed applicant for SUNSHADES, ACRYLIC LENSES, ORDER #SG-01?

The FDA 510(k) record lists Tel-Time Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNSHADES, ACRYLIC LENSES, ORDER #SG-01?

The FDA product code for SUNSHADES, ACRYLIC LENSES, ORDER #SG-01 is HQY.

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 Tel-Time Products 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: 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.

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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