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FDA 510(k)

REGAN-LOWE AGAR

K-Number: K861734 · 1986-05-16

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1986-05-16
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

REGAN-LOWE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1986-05-16 under 510(k) number K861734. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGAN-LOWE AGAR?

REGAN-LOWE AGAR is a medical device that received FDA 510(k) clearance on 1986-05-16. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K861734.

When did REGAN-LOWE AGAR receive FDA 510(k) clearance?

REGAN-LOWE AGAR received FDA 510(k) clearance on 1986-05-16, under 510(k) number K861734.

Who is the listed applicant for REGAN-LOWE AGAR?

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

What is the FDA product code for REGAN-LOWE AGAR?

The FDA product code for REGAN-LOWE AGAR is JSJ.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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Related Devices (Code: JSJ)

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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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