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FDA 510(k)

CYTO-TEK CENTRIFUGE

K-Number: K852117 · 1985-06-10

ApplicantMiles Laboratories, Inc.
Decision Date1985-06-10
Product CodeIFB
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CYTO-TEK CENTRIFUGE is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1985-06-10 under 510(k) number K852117. The device is classified under product code IFB. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYTO-TEK CENTRIFUGE?

CYTO-TEK CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1985-06-10. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K852117.

When did CYTO-TEK CENTRIFUGE receive FDA 510(k) clearance?

CYTO-TEK CENTRIFUGE received FDA 510(k) clearance on 1985-06-10, under 510(k) number K852117.

Who is the listed applicant for CYTO-TEK CENTRIFUGE?

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

What is the FDA product code for CYTO-TEK CENTRIFUGE?

The FDA product code for CYTO-TEK CENTRIFUGE is IFB.

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Related Devices (Code: IFB)

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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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