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FDA 510(k)

MS-2 IDENTIFICATION SYSTEM

K-Number: K802309 · 1980-12-01

ApplicantAbbott Laboratories
Decision Date1980-12-01
Product CodeJXB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MS-2 IDENTIFICATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1980-12-01 under 510(k) number K802309. The device is classified under product code JXB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS-2 IDENTIFICATION SYSTEM?

MS-2 IDENTIFICATION SYSTEM is a medical device that received FDA 510(k) clearance on 1980-12-01. The listed applicant is Abbott Laboratories. The 510(k) number is K802309.

When did MS-2 IDENTIFICATION SYSTEM receive FDA 510(k) clearance?

MS-2 IDENTIFICATION SYSTEM received FDA 510(k) clearance on 1980-12-01, under 510(k) number K802309.

Who is the listed applicant for MS-2 IDENTIFICATION SYSTEM?

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

What is the FDA product code for MS-2 IDENTIFICATION SYSTEM?

The FDA product code for MS-2 IDENTIFICATION SYSTEM is JXB.

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Related Devices (Code: JXB)

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.

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Official Source

View on FDA Database →

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

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