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FDA 510(k)

CLEARVIEW CW-10

K-Number: K870210 · 1987-04-28

ApplicantClearview Instruments, Inc.
Decision Date1987-04-28
Product CodeGKR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CLEARVIEW CW-10 is the device name listed in this FDA 510(k) record. The listed applicant is Clearview Instruments, Inc.. It received FDA 510(k) clearance on 1987-04-28 under 510(k) number K870210. The device is classified under product code GKR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVIEW CW-10?

CLEARVIEW CW-10 is a medical device that received FDA 510(k) clearance on 1987-04-28. The listed applicant is Clearview Instruments, Inc.. The 510(k) number is K870210.

When did CLEARVIEW CW-10 receive FDA 510(k) clearance?

CLEARVIEW CW-10 received FDA 510(k) clearance on 1987-04-28, under 510(k) number K870210.

Who is the listed applicant for CLEARVIEW CW-10?

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

What is the FDA product code for CLEARVIEW CW-10?

The FDA product code for CLEARVIEW CW-10 is GKR.

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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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