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)

HOUSE SUCTION IRRIGATOR

K-Number: K780153 · 1978-02-02

Decision Date1978-02-02
Product CodeJYC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOUSE SUCTION IRRIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1978-02-02 under 510(k) number K780153. The device is classified under product code JYC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOUSE SUCTION IRRIGATOR?

HOUSE SUCTION IRRIGATOR is a medical device that received FDA 510(k) clearance on 1978-02-02. The listed applicant is Edward Weck, Inc.. The 510(k) number is K780153.

When did HOUSE SUCTION IRRIGATOR receive FDA 510(k) clearance?

HOUSE SUCTION IRRIGATOR received FDA 510(k) clearance on 1978-02-02, under 510(k) number K780153.

Who is the listed applicant for HOUSE SUCTION IRRIGATOR?

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

What is the FDA product code for HOUSE SUCTION IRRIGATOR?

The FDA product code for HOUSE SUCTION IRRIGATOR is JYC.

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 Edward Weck, 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 140 devices →

Related Devices (Code: JYC)

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.

↑