PMT MODEL 1110-5 PMT PERITONEAL CATHETER
K-Number: K884036 · 1988-12-22
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Device Summary
Frequently Asked Questions
What is the PMT MODEL 1110-5 PMT PERITONEAL CATHETER?
PMT MODEL 1110-5 PMT PERITONEAL CATHETER is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is Pmt Corp.. The 510(k) number is K884036.
When did PMT MODEL 1110-5 PMT PERITONEAL CATHETER receive FDA 510(k) clearance?
PMT MODEL 1110-5 PMT PERITONEAL CATHETER received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884036.
Who is the listed applicant for PMT MODEL 1110-5 PMT PERITONEAL CATHETER?
The FDA 510(k) record lists Pmt Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PMT MODEL 1110-5 PMT PERITONEAL CATHETER?
The FDA product code for PMT MODEL 1110-5 PMT PERITONEAL CATHETER is JXG.
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 Pmt Corp. 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: JXG)
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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