POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001
K-Number: K983029 · 1999-01-29
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Device Summary
Frequently Asked Questions
What is the POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001?
POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001 is a medical device that received FDA 510(k) clearance on 1999-01-29. The listed applicant is Tpc Advanced Technology, Inc.. The 510(k) number is K983029.
When did POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001 receive FDA 510(k) clearance?
POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001 received FDA 510(k) clearance on 1999-01-29, under 510(k) number K983029.
Who is the listed applicant for POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001?
The FDA 510(k) record lists Tpc Advanced Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001?
The FDA product code for POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001 is ELC.
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 Tpc Advanced Technology, 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: ELC)
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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