THE SIGNATURE SERIES, IC II
K-Number: K933196 · 1994-07-12
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Device Summary
Frequently Asked Questions
What is the THE SIGNATURE SERIES, IC II?
THE SIGNATURE SERIES, IC II is a medical device that received FDA 510(k) clearance on 1994-07-12. The listed applicant is Progressive Electrical Therapeutics. The 510(k) number is K933196.
When did THE SIGNATURE SERIES, IC II receive FDA 510(k) clearance?
THE SIGNATURE SERIES, IC II received FDA 510(k) clearance on 1994-07-12, under 510(k) number K933196.
Who is the listed applicant for THE SIGNATURE SERIES, IC II?
The FDA 510(k) record lists Progressive Electrical Therapeutics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE SIGNATURE SERIES, IC II?
The FDA product code for THE SIGNATURE SERIES, IC II is IPF.
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 Progressive Electrical Therapeutics 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: IPF)
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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