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FDA 510(k)

ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01

K-Number: K990587 · 1999-04-07

ApplicantBio-Rad
Decision Date1999-04-07
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1999-04-07 under 510(k) number K990587. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01?

ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01 is a medical device that received FDA 510(k) clearance on 1999-04-07. The listed applicant is Bio-Rad. The 510(k) number is K990587.

When did ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01 receive FDA 510(k) clearance?

ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01 received FDA 510(k) clearance on 1999-04-07, under 510(k) number K990587.

Who is the listed applicant for ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01?

The FDA product code for ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01 is DHR.

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Related Devices (Code: DHR)

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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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