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FDA 510(k)

ELECTRIC INSTRUMENT TABLE

K-Number: K832073 · 1983-08-12

ApplicantCooperVision, Inc.
Decision Date1983-08-12
Product CodeHMF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ELECTRIC INSTRUMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832073. The device is classified under product code HMF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC INSTRUMENT TABLE?

ELECTRIC INSTRUMENT TABLE is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is CooperVision, Inc.. The 510(k) number is K832073.

When did ELECTRIC INSTRUMENT TABLE receive FDA 510(k) clearance?

ELECTRIC INSTRUMENT TABLE received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832073.

Who is the listed applicant for ELECTRIC INSTRUMENT TABLE?

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

What is the FDA product code for ELECTRIC INSTRUMENT TABLE?

The FDA product code for ELECTRIC INSTRUMENT TABLE is HMF.

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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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