MICRO STIX #011-010-5000 & HOLDER#5100
K-Number: K823833 · 1983-03-08
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Device Summary
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.
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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