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FDA 510(k)

LENSES, CONTACT, POLYMETHYL METHACRYLATE

K-Number: K760213 · 1976-08-09

Decision Date1976-08-09
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

LENSES, CONTACT, POLYMETHYL METHACRYLATE is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Affiliated Labs, Inc.. It received FDA 510(k) clearance on 1976-08-09 under 510(k) number K760213. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LENSES, CONTACT, POLYMETHYL METHACRYLATE?

LENSES, CONTACT, POLYMETHYL METHACRYLATE is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Progressive Affiliated Labs, Inc.. The 510(k) number is K760213.

When did LENSES, CONTACT, POLYMETHYL METHACRYLATE receive FDA 510(k) clearance?

LENSES, CONTACT, POLYMETHYL METHACRYLATE received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760213.

Who is the listed applicant for LENSES, CONTACT, POLYMETHYL METHACRYLATE?

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

What is the FDA product code for LENSES, CONTACT, POLYMETHYL METHACRYLATE?

The FDA product code for LENSES, CONTACT, POLYMETHYL METHACRYLATE is HPX.

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: HPX)

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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