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FDA 510(k)

LEIF CENTRIFUGAL CYTOLOGY BUCKET

K-Number: K792032 · 1979-11-30

ApplicantRobert C. Leif, Ph.D.
Decision Date1979-11-30
Product CodeIFB
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LEIF CENTRIFUGAL CYTOLOGY BUCKET is the device name listed in this FDA 510(k) record. The listed applicant is Robert C. Leif, Ph.D.. It received FDA 510(k) clearance on 1979-11-30 under 510(k) number K792032. 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 LEIF CENTRIFUGAL CYTOLOGY BUCKET?

LEIF CENTRIFUGAL CYTOLOGY BUCKET is a medical device that received FDA 510(k) clearance on 1979-11-30. The listed applicant is Robert C. Leif, Ph.D.. The 510(k) number is K792032.

When did LEIF CENTRIFUGAL CYTOLOGY BUCKET receive FDA 510(k) clearance?

LEIF CENTRIFUGAL CYTOLOGY BUCKET received FDA 510(k) clearance on 1979-11-30, under 510(k) number K792032.

Who is the listed applicant for LEIF CENTRIFUGAL CYTOLOGY BUCKET?

The FDA 510(k) record lists Robert C. Leif, Ph.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEIF CENTRIFUGAL CYTOLOGY BUCKET?

The FDA product code for LEIF CENTRIFUGAL CYTOLOGY BUCKET is IFB.

Related Clinical Trials

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Related Devices (Code: IFB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K852117CYTO-TEK CENTRIFUGEMiles Laboratories, Inc.K810848CYTOBUCKET MODEL 1024Cytochem, Inc.

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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