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FDA 510(k)

MICRO STIX #011-010-5000 & HOLDER#5100

K-Number: K823833 · 1983-03-08

Decision Date1983-03-08
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICRO STIX #011-010-5000 & HOLDER#5100 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1983-03-08 under 510(k) number K823833. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO STIX #011-010-5000 & HOLDER#5100?

MICRO STIX #011-010-5000 & HOLDER#5100 is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is Dynatech Corp.. The 510(k) number is K823833.

When did MICRO STIX #011-010-5000 & HOLDER#5100 receive FDA 510(k) clearance?

MICRO STIX #011-010-5000 & HOLDER#5100 received FDA 510(k) clearance on 1983-03-08, under 510(k) number K823833.

Who is the listed applicant for MICRO STIX #011-010-5000 & HOLDER#5100?

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

What is the FDA product code for MICRO STIX #011-010-5000 & HOLDER#5100?

The FDA product code for MICRO STIX #011-010-5000 & HOLDER#5100 is LIB.

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.

Other records listing Dynatech Corp. as applicant

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.

View all 27 devices →

Related Devices (Code: LIB)

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.

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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