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FDA 510(k)

SPECIFIC ATLAS MICROJUST

K-Number: K833324 · 1983-11-14

ApplicantHaygood Scientific Tool Co.
Decision Date1983-11-14
Product Code
DecisionSubstantially Equivalent

Device Summary

SPECIFIC ATLAS MICROJUST is the device name listed in this FDA 510(k) record. The listed applicant is Haygood Scientific Tool Co.. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833324. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIFIC ATLAS MICROJUST?

SPECIFIC ATLAS MICROJUST is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Haygood Scientific Tool Co.. The 510(k) number is K833324.

When did SPECIFIC ATLAS MICROJUST receive FDA 510(k) clearance?

SPECIFIC ATLAS MICROJUST received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833324.

Who is the listed applicant for SPECIFIC ATLAS MICROJUST?

The FDA 510(k) record lists Haygood Scientific Tool Co. as the applicant. This does not by itself establish the device manufacturer.

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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

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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