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FDA 510(k)

ENTERON ABDOMINAL PARACENTESIS TRAY

K-Number: K874063 · 1987-12-04

ApplicantEndovations
Decision Date1987-12-04
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

ENTERON ABDOMINAL PARACENTESIS TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Endovations. It received FDA 510(k) clearance on 1987-12-04 under 510(k) number K874063. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ENTERON ABDOMINAL PARACENTESIS TRAY?

ENTERON ABDOMINAL PARACENTESIS TRAY is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is Endovations. The 510(k) number is K874063.

When did ENTERON ABDOMINAL PARACENTESIS TRAY receive FDA 510(k) clearance?

ENTERON ABDOMINAL PARACENTESIS TRAY received FDA 510(k) clearance on 1987-12-04, under 510(k) number K874063.

Who is the listed applicant for ENTERON ABDOMINAL PARACENTESIS TRAY?

The FDA 510(k) record lists Endovations as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTERON ABDOMINAL PARACENTESIS TRAY?

The FDA product code for ENTERON ABDOMINAL PARACENTESIS TRAY is KDD.

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 Endovations 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 37 devices →

Related Devices (Code: KDD)

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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