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FDA 510(k)

Blood Collection Accessory (BUCA)

K-Number: K181754 · 2019-07-30

ApplicantNsp Tech Pte, Ltd.
Decision Date2019-07-30
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Blood Collection Accessory (BUCA) is a medical device manufactured by Nsp Tech Pte, Ltd.. It received FDA 510(k) clearance on 2019-07-30 under approval number K181754. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Blood Collection Accessory (BUCA)?

Blood Collection Accessory (BUCA) is a medical device that received FDA 510(k) clearance on 2019-07-30. It is manufactured by Nsp Tech Pte, Ltd.. The 510(k) number is K181754.

When was Blood Collection Accessory (BUCA) approved by the FDA?

Blood Collection Accessory (BUCA) received FDA 510(k) clearance on 2019-07-30, under approval number K181754.

What company makes Blood Collection Accessory (BUCA)?

Blood Collection Accessory (BUCA) is manufactured by Nsp Tech Pte, Ltd..

What is the FDA product code for Blood Collection Accessory (BUCA)?

The FDA product code for Blood Collection Accessory (BUCA) is JKA.

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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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