THAYER MARTIN, MODIFIED PILL POCKET
K-Number: K934331 · 1993-12-21
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Device Summary
Frequently Asked Questions
What is the THAYER MARTIN, MODIFIED PILL POCKET?
THAYER MARTIN, MODIFIED PILL POCKET is a medical device that received FDA 510(k) clearance on 1993-12-21. The listed applicant is Hardy Diagnostics. The 510(k) number is K934331.
When did THAYER MARTIN, MODIFIED PILL POCKET receive FDA 510(k) clearance?
THAYER MARTIN, MODIFIED PILL POCKET received FDA 510(k) clearance on 1993-12-21, under 510(k) number K934331.
Who is the listed applicant for THAYER MARTIN, MODIFIED PILL POCKET?
The FDA 510(k) record lists Hardy Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THAYER MARTIN, MODIFIED PILL POCKET?
The FDA product code for THAYER MARTIN, MODIFIED PILL POCKET 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.
Other records listing Hardy Diagnostics 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: 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.
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