FDA 510(k)

MONOJECT LUER ADAPTER

K-Number: K940961 · 1994-09-14

Decision Date1994-09-14

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MONOJECT LUER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1994-09-14 under 510(k) number K940961. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT LUER ADAPTER?

MONOJECT LUER ADAPTER is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Sherwood Medical Co.. The 510(k) number is K940961.

When did MONOJECT LUER ADAPTER receive FDA 510(k) clearance?

MONOJECT LUER ADAPTER received FDA 510(k) clearance on 1994-09-14, under 510(k) number K940961.

Who is the listed applicant for MONOJECT LUER ADAPTER?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONOJECT LUER ADAPTER?

The FDA product code for MONOJECT LUER ADAPTER is FMI.

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Other records listing Sherwood Medical Co. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.