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)

CEMENT FUME EVACUATOR TANK & FILTER

K-Number: K810542 · 1981-03-13

Decision Date1981-03-13
Product CodeJDY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CEMENT FUME EVACUATOR TANK & FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Walgen Medical Innoventions. It received FDA 510(k) clearance on 1981-03-13 under 510(k) number K810542. The device is classified under product code JDY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENT FUME EVACUATOR TANK & FILTER?

CEMENT FUME EVACUATOR TANK & FILTER is a medical device that received FDA 510(k) clearance on 1981-03-13. The listed applicant is Walgen Medical Innoventions. The 510(k) number is K810542.

When did CEMENT FUME EVACUATOR TANK & FILTER receive FDA 510(k) clearance?

CEMENT FUME EVACUATOR TANK & FILTER received FDA 510(k) clearance on 1981-03-13, under 510(k) number K810542.

Who is the listed applicant for CEMENT FUME EVACUATOR TANK & FILTER?

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

What is the FDA product code for CEMENT FUME EVACUATOR TANK & FILTER?

The FDA product code for CEMENT FUME EVACUATOR TANK & FILTER is JDY.

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 Walgen Medical Innoventions 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: JDY)

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.

↑