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FDA 510(k)

DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE

K-Number: K941206 · 1995-07-25

Decision Date1995-07-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is New Eder Corp.. It received FDA 510(k) clearance on 1995-07-25 under 510(k) number K941206. 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 DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE?

DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is New Eder Corp.. The 510(k) number is K941206.

When did DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE receive FDA 510(k) clearance?

DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE received FDA 510(k) clearance on 1995-07-25, under 510(k) number K941206.

Who is the listed applicant for DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE?

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

What is the FDA product code for DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE?

The FDA product code for DUAL VALVE ASPIRATION/LAVAGE CANNULA AND ASPIRATION/SUCTION PROBE 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 New Eder 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.

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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