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FDA 510(k)

ACRYLIC SHEET, PLEXIGLASS MC

K-Number: K830031 · 1983-01-28

ApplicantSummit Orthodontic Services, Inc.
Decision Date1983-01-28
Product Code
DecisionSubstantially Equivalent

Device Summary

ACRYLIC SHEET, PLEXIGLASS MC is the device name listed in this FDA 510(k) record. The listed applicant is Summit Orthodontic Services, Inc.. It received FDA 510(k) clearance on 1983-01-28 under 510(k) number K830031. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRYLIC SHEET, PLEXIGLASS MC?

ACRYLIC SHEET, PLEXIGLASS MC is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Summit Orthodontic Services, Inc.. The 510(k) number is K830031.

When did ACRYLIC SHEET, PLEXIGLASS MC receive FDA 510(k) clearance?

ACRYLIC SHEET, PLEXIGLASS MC received FDA 510(k) clearance on 1983-01-28, under 510(k) number K830031.

Who is the listed applicant for ACRYLIC SHEET, PLEXIGLASS MC?

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

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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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