FDA 510(k)

MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT

K-Number: K894511 · 1989-10-17

ApplicantIntl. Ophthalmic Industries Corp.

Decision Date1989-10-17

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Ophthalmic Industries Corp.. It received FDA 510(k) clearance on 1989-10-17 under 510(k) number K894511. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT?

MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT is a medical device that received FDA 510(k) clearance on 1989-10-17. The listed applicant is Intl. Ophthalmic Industries Corp.. The 510(k) number is K894511.

When did MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT receive FDA 510(k) clearance?

MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT received FDA 510(k) clearance on 1989-10-17, under 510(k) number K894511.

Who is the listed applicant for MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT?

The FDA 510(k) record lists Intl. Ophthalmic Industries Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT?

The FDA product code for MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT is HQC.

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Other records listing Intl. Ophthalmic Industries Corp. as applicant

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Related Devices (Code: HQC)

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Official Source

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