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FDA 510(k)

ASPIRATION REVERSAL CONTROL (ARC) MODULE

K-Number: K870068 · 1987-02-12

ApplicantOptical Micro Systems, Inc.
Decision Date1987-02-12
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ASPIRATION REVERSAL CONTROL (ARC) MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Optical Micro Systems, Inc.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K870068. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATION REVERSAL CONTROL (ARC) MODULE?

ASPIRATION REVERSAL CONTROL (ARC) MODULE is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Optical Micro Systems, Inc.. The 510(k) number is K870068.

When did ASPIRATION REVERSAL CONTROL (ARC) MODULE receive FDA 510(k) clearance?

ASPIRATION REVERSAL CONTROL (ARC) MODULE received FDA 510(k) clearance on 1987-02-12, under 510(k) number K870068.

Who is the listed applicant for ASPIRATION REVERSAL CONTROL (ARC) MODULE?

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

What is the FDA product code for ASPIRATION REVERSAL CONTROL (ARC) MODULE?

The FDA product code for ASPIRATION REVERSAL CONTROL (ARC) MODULE is HQE.

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Other records listing Optical Micro Systems, Inc. as applicant

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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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