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FDA 510(k)

CONTACT PLATE LECITHIN & POLYSORBATE 80

K-Number: K830063 · 1983-02-09

Decision Date1983-02-09
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CONTACT PLATE LECITHIN & POLYSORBATE 80 is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1983-02-09 under 510(k) number K830063. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT PLATE LECITHIN & POLYSORBATE 80?

CONTACT PLATE LECITHIN & POLYSORBATE 80 is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is bioMerieux, Inc.. The 510(k) number is K830063.

When did CONTACT PLATE LECITHIN & POLYSORBATE 80 receive FDA 510(k) clearance?

CONTACT PLATE LECITHIN & POLYSORBATE 80 received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830063.

Who is the listed applicant for CONTACT PLATE LECITHIN & POLYSORBATE 80?

The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTACT PLATE LECITHIN & POLYSORBATE 80?

The FDA product code for CONTACT PLATE LECITHIN & POLYSORBATE 80 is JSG.

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 bioMerieux, Inc. 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 248 devices →

Related Devices (Code: JSG)

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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