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FDA 510(k)

AFT(R) HEP PERFORMANCE EVALUATION PROGRAM

K-Number: K865019 · 1987-02-10

ApplicantBehring Diagnostics, Inc.
Decision Date1987-02-10
Product Code
DecisionSubstantially Equivalent

Device Summary

AFT(R) HEP PERFORMANCE EVALUATION PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K865019. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFT(R) HEP PERFORMANCE EVALUATION PROGRAM?

AFT(R) HEP PERFORMANCE EVALUATION PROGRAM is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K865019.

When did AFT(R) HEP PERFORMANCE EVALUATION PROGRAM receive FDA 510(k) clearance?

AFT(R) HEP PERFORMANCE EVALUATION PROGRAM received FDA 510(k) clearance on 1987-02-10, under 510(k) number K865019.

Who is the listed applicant for AFT(R) HEP PERFORMANCE EVALUATION PROGRAM?

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

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Other records listing Behring Diagnostics, Inc. as applicant

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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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