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FDA 510(k)

Blood Collection Accessory (BUCA)

K-Number: K181754 · 2019-07-30

Decision Date2019-07-30
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Blood Collection Accessory (BUCA) is the device name listed in this FDA 510(k) record. The listed applicant is Nsp Tech Pte, Ltd.. It received FDA 510(k) clearance on 2019-07-30 under 510(k) 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. The listed applicant is Nsp Tech Pte, Ltd.. The 510(k) number is K181754.

When did Blood Collection Accessory (BUCA) receive FDA 510(k) clearance?

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

Who is the listed applicant for Blood Collection Accessory (BUCA)?

The FDA 510(k) record lists Nsp Tech Pte, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Nsp Tech Pte, Ltd. 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.

Related Devices (Code: JKA)

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

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