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FDA 510(k)

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE

K-Number: K843314 · 1984-09-27

Decision Date1984-09-27
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Mpl Division. It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843314. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE?

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Smith & Nephew, Mpl Division. The 510(k) number is K843314.

When did MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE receive FDA 510(k) clearance?

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843314.

Who is the listed applicant for MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE?

The FDA 510(k) record lists Smith & Nephew, Mpl Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE?

The FDA product code for MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE is EJI.

Related Clinical Trials

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.

Other records listing Smith & Nephew, Mpl Division 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.

View all 9 devices →

Related Devices (Code: EJI)

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

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