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FDA 510(k)

CYTOASPIRATOR

K-Number: K902910 · 1991-01-16

ApplicantH & B Medical Technology, Inc.
Decision Date1991-01-16
Product CodeFCK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CYTOASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is H & B Medical Technology, Inc.. It received FDA 510(k) clearance on 1991-01-16 under 510(k) number K902910. The device is classified under product code FCK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYTOASPIRATOR?

CYTOASPIRATOR is a medical device that received FDA 510(k) clearance on 1991-01-16. The listed applicant is H & B Medical Technology, Inc.. The 510(k) number is K902910.

When did CYTOASPIRATOR receive FDA 510(k) clearance?

CYTOASPIRATOR received FDA 510(k) clearance on 1991-01-16, under 510(k) number K902910.

Who is the listed applicant for CYTOASPIRATOR?

The FDA 510(k) record lists H & B Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYTOASPIRATOR?

The FDA product code for CYTOASPIRATOR is FCK.

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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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