FDA 510(k)

LASERSPEC

K-Number: K841430 · 1984-12-13

Decision Date1984-12-13

Product Code

DecisionSubstantially Equivalent

Device Summary

LASERSPEC is the device name listed in this FDA 510(k) record. The listed applicant is Clement Clarke, Inc.. It received FDA 510(k) clearance on 1984-12-13 under 510(k) number K841430. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERSPEC?

LASERSPEC is a medical device that received FDA 510(k) clearance on 1984-12-13. The listed applicant is Clement Clarke, Inc.. The 510(k) number is K841430.

When did LASERSPEC receive FDA 510(k) clearance?

LASERSPEC received FDA 510(k) clearance on 1984-12-13, under 510(k) number K841430.

Who is the listed applicant for LASERSPEC?

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

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Other records listing Clement Clarke, Inc. as applicant

K961512PERKINS HAND-HELD APPLANATION TONOMETER K952713MINI WRIGHT LR AFS K953965904 SLIT LAMP K932258OPTICOM M600 K914126VMX MINI-LOG FLOWMETER K914896FRIEDMANN ANALYSER 3

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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.