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FDA 510(k)

SMB Luer lock disposable syringe

K-Number: K231558 · 2024-01-12

Decision Date2024-01-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SMB Luer lock disposable syringe is the device name listed in this FDA 510(k) record. The listed applicant is Smb Corporation of India. It received FDA 510(k) clearance on 2024-01-12 under 510(k) number K231558. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMB Luer lock disposable syringe?

SMB Luer lock disposable syringe is a medical device that received FDA 510(k) clearance on 2024-01-12. The listed applicant is Smb Corporation of India. The 510(k) number is K231558.

When did SMB Luer lock disposable syringe receive FDA 510(k) clearance?

SMB Luer lock disposable syringe received FDA 510(k) clearance on 2024-01-12, under 510(k) number K231558.

Who is the listed applicant for SMB Luer lock disposable syringe?

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

What is the FDA product code for SMB Luer lock disposable syringe?

The FDA product code for SMB Luer lock disposable syringe is FMF.

Related Devices (Code: FMF)

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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