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FDA 510(k)

MT-336 AUTOMATIC PERIMETER

K-Number: K902878 · 1990-09-18

ApplicantMarco Technologies
Decision Date1990-09-18
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MT-336 AUTOMATIC PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Marco Technologies. It received FDA 510(k) clearance on 1990-09-18 under 510(k) number K902878. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT-336 AUTOMATIC PERIMETER?

MT-336 AUTOMATIC PERIMETER is a medical device that received FDA 510(k) clearance on 1990-09-18. The listed applicant is Marco Technologies. The 510(k) number is K902878.

When did MT-336 AUTOMATIC PERIMETER receive FDA 510(k) clearance?

MT-336 AUTOMATIC PERIMETER received FDA 510(k) clearance on 1990-09-18, under 510(k) number K902878.

Who is the listed applicant for MT-336 AUTOMATIC PERIMETER?

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

What is the FDA product code for MT-336 AUTOMATIC PERIMETER?

The FDA product code for MT-336 AUTOMATIC PERIMETER is HPT.

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Related Devices (Code: HPT)

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

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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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