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FDA 510(k)

Z VIEW METER MODEL 300

K-Number: K830823 · 1983-05-18

ApplicantLintronics Industries, Inc.
Decision Date1983-05-18
Product CodeKRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Z VIEW METER MODEL 300 is the device name listed in this FDA 510(k) record. The listed applicant is Lintronics Industries, Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K830823. The device is classified under product code KRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z VIEW METER MODEL 300?

Z VIEW METER MODEL 300 is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Lintronics Industries, Inc.. The 510(k) number is K830823.

When did Z VIEW METER MODEL 300 receive FDA 510(k) clearance?

Z VIEW METER MODEL 300 received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830823.

Who is the listed applicant for Z VIEW METER MODEL 300?

The FDA 510(k) record lists Lintronics Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Z VIEW METER MODEL 300?

The FDA product code for Z VIEW METER MODEL 300 is KRC.

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Related Devices (Code: KRC)

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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