FDA 510(k)

PANPAC DISPOSABLE VACUUM CURETTES

K-Number: K161106 · 2017-01-13

Decision Date2017-01-13

Product CodeHGH

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

PANPAC DISPOSABLE VACUUM CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is Panpac Medical Corporation. It received FDA 510(k) clearance on 2017-01-13 under 510(k) number K161106. The device is classified under product code HGH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANPAC DISPOSABLE VACUUM CURETTES?

PANPAC DISPOSABLE VACUUM CURETTES is a medical device that received FDA 510(k) clearance on 2017-01-13. The listed applicant is Panpac Medical Corporation. The 510(k) number is K161106.

When did PANPAC DISPOSABLE VACUUM CURETTES receive FDA 510(k) clearance?

PANPAC DISPOSABLE VACUUM CURETTES received FDA 510(k) clearance on 2017-01-13, under 510(k) number K161106.

Who is the listed applicant for PANPAC DISPOSABLE VACUUM CURETTES?

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

What is the FDA product code for PANPAC DISPOSABLE VACUUM CURETTES?

The FDA product code for PANPAC DISPOSABLE VACUUM CURETTES is HGH.

Other records listing Panpac Medical Corporation 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.

K173351Panpac Flexi Shelf Pessary K153422Panpac Disposable Pessary Fitting Set

Related Devices (Code: HGH)

K172151Hysteroscopy SystemChongquin Jinshan Science & Technology (Group) Co., Ltd.

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.