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FDA 510(k)

PMT MODEL 1110-5 PMT PERITONEAL CATHETER

K-Number: K884036 · 1988-12-22

ApplicantPmt Corp.
Decision Date1988-12-22
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT MODEL 1110-5 PMT PERITONEAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1988-12-22 under 510(k) number K884036. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 20 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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