IMPROVED THAYER-MARTIN MEDIUM
K-Number: K770925 · 1977-06-08
Advertisement
Device Summary
Frequently Asked Questions
What is the IMPROVED THAYER-MARTIN MEDIUM?
IMPROVED THAYER-MARTIN MEDIUM is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Micro-Tech Diagnostic, Inc.. The 510(k) number is K770925.
When did IMPROVED THAYER-MARTIN MEDIUM receive FDA 510(k) clearance?
IMPROVED THAYER-MARTIN MEDIUM received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770925.
Who is the listed applicant for IMPROVED THAYER-MARTIN MEDIUM?
The FDA 510(k) record lists Micro-Tech Diagnostic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMPROVED THAYER-MARTIN MEDIUM?
The FDA product code for IMPROVED THAYER-MARTIN MEDIUM is JTY.
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.
Related Devices (Code: JTY)
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.
Advertisement