INDXTM DIP-S-TICKSTM
K-Number: K920569 · 1993-02-09
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Device Summary
Frequently Asked Questions
What is the INDXTM DIP-S-TICKSTM?
INDXTM DIP-S-TICKSTM is a medical device that received FDA 510(k) clearance on 1993-02-09. The listed applicant is Intercare Diagnostics, Inc.. The 510(k) number is K920569.
When did INDXTM DIP-S-TICKSTM receive FDA 510(k) clearance?
INDXTM DIP-S-TICKSTM received FDA 510(k) clearance on 1993-02-09, under 510(k) number K920569.
Who is the listed applicant for INDXTM DIP-S-TICKSTM?
The FDA 510(k) record lists Intercare Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INDXTM DIP-S-TICKSTM?
The FDA product code for INDXTM DIP-S-TICKSTM is LSQ.
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 Intercare Diagnostics, Inc. 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: LSQ)
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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