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FDA 510(k)

HYSTEROSER

K-Number: K791330 · 1980-03-03

ApplicantA. B. Vacuum Extractor, Inc.
Decision Date1980-03-03
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYSTEROSER is the device name listed in this FDA 510(k) record. The listed applicant is A. B. Vacuum Extractor, Inc.. It received FDA 510(k) clearance on 1980-03-03 under 510(k) number K791330. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYSTEROSER?

HYSTEROSER is a medical device that received FDA 510(k) clearance on 1980-03-03. The listed applicant is A. B. Vacuum Extractor, Inc.. The 510(k) number is K791330.

When did HYSTEROSER receive FDA 510(k) clearance?

HYSTEROSER received FDA 510(k) clearance on 1980-03-03, under 510(k) number K791330.

Who is the listed applicant for HYSTEROSER?

The FDA 510(k) record lists A. B. Vacuum Extractor, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYSTEROSER?

The FDA product code for HYSTEROSER is HIH.

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Related Devices (Code: HIH)

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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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