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FDA 510(k)

DISPOS. MONITORING SYS/LI ET AL

K-Number: K820201 · 1982-02-12

ApplicantLinton Biomed Corp.
Decision Date1982-02-12
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOS. MONITORING SYS/LI ET AL is the device name listed in this FDA 510(k) record. The listed applicant is Linton Biomed Corp.. It received FDA 510(k) clearance on 1982-02-12 under 510(k) number K820201. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS. MONITORING SYS/LI ET AL?

DISPOS. MONITORING SYS/LI ET AL is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is Linton Biomed Corp.. The 510(k) number is K820201.

When did DISPOS. MONITORING SYS/LI ET AL receive FDA 510(k) clearance?

DISPOS. MONITORING SYS/LI ET AL received FDA 510(k) clearance on 1982-02-12, under 510(k) number K820201.

Who is the listed applicant for DISPOS. MONITORING SYS/LI ET AL?

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

What is the FDA product code for DISPOS. MONITORING SYS/LI ET AL?

The FDA product code for DISPOS. MONITORING SYS/LI ET AL is DRS.

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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.

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