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FDA 510(k)

VABRA ABORTION UNIT

K-Number: K780387 · 1978-04-12

ApplicantCooper Laboratories
Decision Date1978-04-12
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VABRA ABORTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Laboratories. It received FDA 510(k) clearance on 1978-04-12 under 510(k) number K780387. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VABRA ABORTION UNIT?

VABRA ABORTION UNIT is a medical device that received FDA 510(k) clearance on 1978-04-12. The listed applicant is Cooper Laboratories. The 510(k) number is K780387.

When did VABRA ABORTION UNIT receive FDA 510(k) clearance?

VABRA ABORTION UNIT received FDA 510(k) clearance on 1978-04-12, under 510(k) number K780387.

Who is the listed applicant for VABRA ABORTION UNIT?

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

What is the FDA product code for VABRA ABORTION UNIT?

The FDA product code for VABRA ABORTION UNIT is HHI.

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Related Devices (Code: HHI)

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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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