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FDA 510(k)

AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904

K-Number: K881129 · 1988-06-14

ApplicantBoehringer Laboratories
Decision Date1988-06-14
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904 is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1988-06-14 under 510(k) number K881129. 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 INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904?

AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904 is a medical device that received FDA 510(k) clearance on 1988-06-14. The listed applicant is Boehringer Laboratories. The 510(k) number is K881129.

When did AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904 receive FDA 510(k) clearance?

AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904 received FDA 510(k) clearance on 1988-06-14, under 510(k) number K881129.

Who is the listed applicant for AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904?

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 INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904?

The FDA product code for AUTO-VAC INTRAOPERATIVE AUTOTRANS. RESERVOIR #7904 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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