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)

LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM

K-Number: K052797 · 2006-02-13

Decision Date2006-02-13
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM is the device name listed in this FDA 510(k) record. The listed applicant is Medtek Devices, Inc.. It received FDA 510(k) clearance on 2006-02-13 under 510(k) number K052797. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM?

LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM is a medical device that received FDA 510(k) clearance on 2006-02-13. The listed applicant is Medtek Devices, Inc.. The 510(k) number is K052797.

When did LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM receive FDA 510(k) clearance?

LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM received FDA 510(k) clearance on 2006-02-13, under 510(k) number K052797.

Who is the listed applicant for LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM?

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

What is the FDA product code for LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM?

The FDA product code for LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM is FYD.

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 Medtek Devices, 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.

Related Devices (Code: FYD)

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.

↑