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FDA 510(k)

BLOOD POOL & SUBVETINAL FLUID ASPIRATOR

K-Number: K813274 · 1982-02-05

ApplicantOptical Micro Systems, Inc.
Decision Date1982-02-05
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BLOOD POOL & SUBVETINAL FLUID ASPIRATOR 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 1982-02-05 under 510(k) number K813274. 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 BLOOD POOL & SUBVETINAL FLUID ASPIRATOR?

BLOOD POOL & SUBVETINAL FLUID ASPIRATOR is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Optical Micro Systems, Inc.. The 510(k) number is K813274.

When did BLOOD POOL & SUBVETINAL FLUID ASPIRATOR receive FDA 510(k) clearance?

BLOOD POOL & SUBVETINAL FLUID ASPIRATOR received FDA 510(k) clearance on 1982-02-05, under 510(k) number K813274.

Who is the listed applicant for BLOOD POOL & SUBVETINAL FLUID ASPIRATOR?

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 BLOOD POOL & SUBVETINAL FLUID ASPIRATOR?

The FDA product code for BLOOD POOL & SUBVETINAL FLUID ASPIRATOR is HQE.

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Other records listing Optical Micro Systems, Inc. as applicant

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Related Devices (Code: HQE)

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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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