NeuroLine Disposable Cranial Perforator with Hudson end
K-Number: K213228 · 2022-06-20
Decision Date2022-06-20
Product CodeHBF
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NeuroLine Disposable Cranial Perforator with Hudson end is a medical device manufactured by Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft.. It received FDA 510(k) clearance on 2022-06-20 under approval number K213228. The device is classified under product code HBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NeuroLine Disposable Cranial Perforator with Hudson end?
NeuroLine Disposable Cranial Perforator with Hudson end is a medical device that received FDA 510(k) clearance on 2022-06-20. It is manufactured by Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft.. The 510(k) number is K213228.
When was NeuroLine Disposable Cranial Perforator with Hudson end approved by the FDA?
NeuroLine Disposable Cranial Perforator with Hudson end received FDA 510(k) clearance on 2022-06-20, under approval number K213228.
What company makes NeuroLine Disposable Cranial Perforator with Hudson end?
NeuroLine Disposable Cranial Perforator with Hudson end is manufactured by Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft..
What is the FDA product code for NeuroLine Disposable Cranial Perforator with Hudson end?
The FDA product code for NeuroLine Disposable Cranial Perforator with Hudson end is HBF.
Related Devices (Code: HBF)
Official Source
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