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FDA 510(k)

TUTTIFRUTTI (NON-PRES. SUNGLASSES)

K-Number: K801922 · 1980-11-12

Decision Date1980-11-12
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TUTTIFRUTTI (NON-PRES. SUNGLASSES) is the device name listed in this FDA 510(k) record. The listed applicant is Safety Plastics of New York. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K801922. 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 TUTTIFRUTTI (NON-PRES. SUNGLASSES)?

TUTTIFRUTTI (NON-PRES. SUNGLASSES) is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Safety Plastics of New York. The 510(k) number is K801922.

When did TUTTIFRUTTI (NON-PRES. SUNGLASSES) receive FDA 510(k) clearance?

TUTTIFRUTTI (NON-PRES. SUNGLASSES) received FDA 510(k) clearance on 1980-11-12, under 510(k) number K801922.

Who is the listed applicant for TUTTIFRUTTI (NON-PRES. SUNGLASSES)?

The FDA 510(k) record lists Safety Plastics of New York as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUTTIFRUTTI (NON-PRES. SUNGLASSES)?

The FDA product code for TUTTIFRUTTI (NON-PRES. SUNGLASSES) 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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