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FDA 510(k)

VACO SUCTION ELECTRODE UNIT

K-Number: K860758 · 1986-05-02

ApplicantZimmer Elektromedizin GmbH
Decision Date1986-05-02
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VACO SUCTION ELECTRODE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Elektromedizin GmbH. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K860758. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACO SUCTION ELECTRODE UNIT?

VACO SUCTION ELECTRODE UNIT is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Zimmer Elektromedizin GmbH. The 510(k) number is K860758.

When did VACO SUCTION ELECTRODE UNIT receive FDA 510(k) clearance?

VACO SUCTION ELECTRODE UNIT received FDA 510(k) clearance on 1986-05-02, under 510(k) number K860758.

Who is the listed applicant for VACO SUCTION ELECTRODE UNIT?

The FDA 510(k) record lists Zimmer Elektromedizin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACO SUCTION ELECTRODE UNIT?

The FDA product code for VACO SUCTION ELECTRODE UNIT is IPF.

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Other records listing Zimmer Elektromedizin GmbH as applicant

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Related Devices (Code: IPF)

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.

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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.

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