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FDA 510(k)

CYTOBUCKET MODEL 1024

K-Number: K810848 · 1981-04-23

ApplicantCytochem, Inc.
Decision Date1981-04-23
Product CodeIFB
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CYTOBUCKET MODEL 1024 is the device name listed in this FDA 510(k) record. The listed applicant is Cytochem, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810848. 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 CYTOBUCKET MODEL 1024?

CYTOBUCKET MODEL 1024 is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Cytochem, Inc.. The 510(k) number is K810848.

When did CYTOBUCKET MODEL 1024 receive FDA 510(k) clearance?

CYTOBUCKET MODEL 1024 received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810848.

Who is the listed applicant for CYTOBUCKET MODEL 1024?

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

What is the FDA product code for CYTOBUCKET MODEL 1024?

The FDA product code for CYTOBUCKET MODEL 1024 is IFB.

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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.K792032LEIF CENTRIFUGAL CYTOLOGY BUCKETRobert C. Leif, Ph.D.

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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