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FDA 510(k)

P & T MEDIUM

K-Number: K831059 · 1983-04-28

ApplicantAmerican Micro Scan
Decision Date1983-04-28
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

P & T MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is American Micro Scan. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831059. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P & T MEDIUM?

P & T MEDIUM is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is American Micro Scan. The 510(k) number is K831059.

When did P & T MEDIUM receive FDA 510(k) clearance?

P & T MEDIUM received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831059.

Who is the listed applicant for P & T MEDIUM?

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

What is the FDA product code for P & T MEDIUM?

The FDA product code for P & T MEDIUM is JSM.

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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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