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FDA 510(k)

LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE

K-Number: K930756 · 1994-03-09

Decision Date1994-03-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Endo Technic Corp.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K930756. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE?

LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is Endo Technic Corp.. The 510(k) number is K930756.

When did LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE receive FDA 510(k) clearance?

LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE received FDA 510(k) clearance on 1994-03-09, under 510(k) number K930756.

Who is the listed applicant for LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE?

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

What is the FDA product code for LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE?

The FDA product code for LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE is HET.

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 Endo Technic 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 10 devices →

Related Devices (Code: HET)

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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