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FDA 510(k)

UTERINE VACUM ASPIRATING CURRETTE

K-Number: K802360 · 1980-10-31

Decision Date1980-10-31
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UTERINE VACUM ASPIRATING CURRETTE is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802360. 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 UTERINE VACUM ASPIRATING CURRETTE?

UTERINE VACUM ASPIRATING CURRETTE is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K802360.

When did UTERINE VACUM ASPIRATING CURRETTE receive FDA 510(k) clearance?

UTERINE VACUM ASPIRATING CURRETTE received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802360.

Who is the listed applicant for UTERINE VACUM ASPIRATING CURRETTE?

The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UTERINE VACUM ASPIRATING CURRETTE?

The FDA product code for UTERINE VACUM ASPIRATING CURRETTE is HHI.

Related Clinical Trials

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.

Other records listing American Hospital Supply 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.

View all 56 devices →

Related Devices (Code: HHI)

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.

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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