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FDA 510(k)

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER

K-Number: K827577 · 1983-01-24

ApplicantRandwal Instrument Co., Inc.
Decision Date1983-01-24
Product Code
DecisionSubstantially Equivalent

Device Summary

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Randwal Instrument Co., Inc.. It received FDA 510(k) clearance on 1983-01-24 under 510(k) number K827577. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER?

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER is a medical device that received FDA 510(k) clearance on 1983-01-24. The listed applicant is Randwal Instrument Co., Inc.. The 510(k) number is K827577.

When did VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER receive FDA 510(k) clearance?

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER received FDA 510(k) clearance on 1983-01-24, under 510(k) number K827577.

Who is the listed applicant for VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER?

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

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Other records listing Randwal Instrument Co., 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.

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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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