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FDA 510(k)

VABRA ASPIRATOR

K-Number: K800833 · 1980-05-14

ApplicantCooper Medical Devices Corp.
Decision Date1980-05-14
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VABRA ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Medical Devices Corp.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800833. 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 ASPIRATOR?

VABRA ASPIRATOR is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Cooper Medical Devices Corp.. The 510(k) number is K800833.

When did VABRA ASPIRATOR receive FDA 510(k) clearance?

VABRA ASPIRATOR received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800833.

Who is the listed applicant for VABRA ASPIRATOR?

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

What is the FDA product code for VABRA ASPIRATOR?

The FDA product code for VABRA ASPIRATOR is HHI.

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Other records listing Cooper Medical Devices Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K802927SEBESTYEN IRRIGATING CONTACT LENSK802971LANDERS CONTACT LENSK801850CHARLES PNEUMATIC INTRAOCULAR SCISSORSK801411MAY ILLUMINATED/INFUSION PICK801312THE PROTECTORSK791898OCUTOME MODEL 8000

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Related Devices (Code: HHI)

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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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