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FDA 510(k)

PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE

K-Number: K850046 · 1985-04-15

Decision Date1985-04-15
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE is the device name listed in this FDA 510(k) record. The listed applicant is Professional Supplies, Inc.. It received FDA 510(k) clearance on 1985-04-15 under 510(k) number K850046. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE?

PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE is a medical device that received FDA 510(k) clearance on 1985-04-15. The listed applicant is Professional Supplies, Inc.. The 510(k) number is K850046.

When did PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE receive FDA 510(k) clearance?

PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE received FDA 510(k) clearance on 1985-04-15, under 510(k) number K850046.

Who is the listed applicant for PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE?

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

What is the FDA product code for PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE?

The FDA product code for PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE 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.

Other records listing Professional Supplies, Inc. 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: 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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