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FDA 510(k)

ERCO-VAC -C

K-Number: K990006 · 1999-02-24

ApplicantErcons, Inc.
Decision Date1999-02-24
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ERCO-VAC -C is the device name listed in this FDA 510(k) record. The listed applicant is Ercons, Inc.. It received FDA 510(k) clearance on 1999-02-24 under 510(k) number K990006. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERCO-VAC -C?

ERCO-VAC -C is a medical device that received FDA 510(k) clearance on 1999-02-24. The listed applicant is Ercons, Inc.. The 510(k) number is K990006.

When did ERCO-VAC -C receive FDA 510(k) clearance?

ERCO-VAC -C received FDA 510(k) clearance on 1999-02-24, under 510(k) number K990006.

Who is the listed applicant for ERCO-VAC -C?

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

What is the FDA product code for ERCO-VAC -C?

The FDA product code for ERCO-VAC -C is LKY.

Other records listing Ercons, 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: LKY)

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.

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