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FDA 510(k)

PERCI

K-Number: K780838 · 1978-07-17

ApplicantMicro Tronics Corp.
Decision Date1978-07-17
Product CodeBXX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERCI is the device name listed in this FDA 510(k) record. The listed applicant is Micro Tronics Corp.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K780838. The device is classified under product code BXX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCI?

PERCI is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Micro Tronics Corp.. The 510(k) number is K780838.

When did PERCI receive FDA 510(k) clearance?

PERCI received FDA 510(k) clearance on 1978-07-17, under 510(k) number K780838.

Who is the listed applicant for PERCI?

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

What is the FDA product code for PERCI?

The FDA product code for PERCI is BXX.

Related Clinical Trials

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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Other records listing Micro Tronics Corp. as applicant

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Related Devices (Code: BXX)

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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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