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FDA 510(k)

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I

K-Number: K981213 · 1998-07-01

ApplicantRadionics, Inc.
Decision Date1998-07-01
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1998-07-01 under 510(k) number K981213. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I?

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I is a medical device that received FDA 510(k) clearance on 1998-07-01. The listed applicant is Radionics, Inc.. The 510(k) number is K981213.

When did UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I receive FDA 510(k) clearance?

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I received FDA 510(k) clearance on 1998-07-01, under 510(k) number K981213.

Who is the listed applicant for UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I?

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

What is the FDA product code for UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I?

The FDA product code for UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I is HAW.

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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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