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FDA 510(k)

AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900

K-Number: K862684 · 1986-10-17

ApplicantBoehringer Laboratories
Decision Date1986-10-17
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900 is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1986-10-17 under 510(k) number K862684. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900?

AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900 is a medical device that received FDA 510(k) clearance on 1986-10-17. The listed applicant is Boehringer Laboratories. The 510(k) number is K862684.

When did AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900 receive FDA 510(k) clearance?

AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900 received FDA 510(k) clearance on 1986-10-17, under 510(k) number K862684.

Who is the listed applicant for AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900?

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

What is the FDA product code for AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900?

The FDA product code for AUTO-VAC (TM) AUTOTRANSFUSION RESERV, MODEL 7900 is CAC.

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Related Devices (Code: CAC)

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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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