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FDA 510(k)

HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON.

K-Number: K880963 · 1988-06-24

ApplicantBuckman Co., Inc.
Decision Date1988-06-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON. is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1988-06-24 under 510(k) number K880963. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON.?

HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON. is a medical device that received FDA 510(k) clearance on 1988-06-24. The listed applicant is Buckman Co., Inc.. The 510(k) number is K880963.

When did HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON. receive FDA 510(k) clearance?

HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON. received FDA 510(k) clearance on 1988-06-24, under 510(k) number K880963.

Who is the listed applicant for HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON.?

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

What is the FDA product code for HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON.?

The FDA product code for HAC AUTOLOGY CENTERS DISPENSING KIT FOR FIB.CON. is FMF.

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Related Devices (Code: FMF)

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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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