PANPAC DISPOSABLE VACUUM CURETTES
K-Number: K161106 · 2017-01-13
ApplicantPanpac Medical Corporation
Decision Date2017-01-13
Product CodeHGH
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
PANPAC DISPOSABLE VACUUM CURETTES is a medical device manufactured by Panpac Medical Corporation. It received FDA 510(k) clearance on 2017-01-13 under approval 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. It is manufactured by Panpac Medical Corporation. The 510(k) number is K161106.
When was PANPAC DISPOSABLE VACUUM CURETTES approved by the FDA?
PANPAC DISPOSABLE VACUUM CURETTES received FDA 510(k) clearance on 2017-01-13, under approval number K161106.
What company makes PANPAC DISPOSABLE VACUUM CURETTES?
PANPAC DISPOSABLE VACUUM CURETTES is manufactured by Panpac Medical Corporation.
What is the FDA product code for PANPAC DISPOSABLE VACUUM CURETTES?
The FDA product code for PANPAC DISPOSABLE VACUUM CURETTES is HGH.
Other Devices by Panpac Medical Corporation
Related Devices (Code: HGH)
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.