Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM

K-Number: K902722 · 1990-11-16

ApplicantDavol, Inc.
Decision Date1990-11-16
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1990-11-16 under 510(k) number K902722. 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 BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM?

BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-16. The listed applicant is Davol, Inc.. The 510(k) number is K902722.

When did BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM receive FDA 510(k) clearance?

BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM received FDA 510(k) clearance on 1990-11-16, under 510(k) number K902722.

Who is the listed applicant for BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM?

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

What is the FDA product code for BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM?

The FDA product code for BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM 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 Davol, Inc. 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 50 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

View on FDA Database →

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

↑