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FDA 510(k)

MEDTEK #411 PORTABLE B-P INSTR.

K-Number: K800614 · 1980-04-02

ApplicantMed-Tek Corp.
Decision Date1980-04-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTEK #411 PORTABLE B-P INSTR. is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tek Corp.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800614. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTEK #411 PORTABLE B-P INSTR.?

MEDTEK #411 PORTABLE B-P INSTR. is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Med-Tek Corp.. The 510(k) number is K800614.

When did MEDTEK #411 PORTABLE B-P INSTR. receive FDA 510(k) clearance?

MEDTEK #411 PORTABLE B-P INSTR. received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800614.

Who is the listed applicant for MEDTEK #411 PORTABLE B-P INSTR.?

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

What is the FDA product code for MEDTEK #411 PORTABLE B-P INSTR.?

The FDA product code for MEDTEK #411 PORTABLE B-P INSTR. is DXN.

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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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