Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

THAYER MARTIN, MODIFIED PILL POCKET

K-Number: K934331 · 1993-12-21

Decision Date1993-12-21
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER MARTIN, MODIFIED PILL POCKET is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Diagnostics. It received FDA 510(k) clearance on 1993-12-21 under 510(k) number K934331. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 108 devices →

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.

↑