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FDA 510(k)

LYSINE IRON AGAR (LIA) PRODUCT #T3046

K-Number: K873703 · 1987-10-02

ApplicantLakewood Biochemical Co., Inc.
Decision Date1987-10-02
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LYSINE IRON AGAR (LIA) PRODUCT #T3046 is the device name listed in this FDA 510(k) record. The listed applicant is Lakewood Biochemical Co., Inc.. It received FDA 510(k) clearance on 1987-10-02 under 510(k) number K873703. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYSINE IRON AGAR (LIA) PRODUCT #T3046?

LYSINE IRON AGAR (LIA) PRODUCT #T3046 is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K873703.

When did LYSINE IRON AGAR (LIA) PRODUCT #T3046 receive FDA 510(k) clearance?

LYSINE IRON AGAR (LIA) PRODUCT #T3046 received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873703.

Who is the listed applicant for LYSINE IRON AGAR (LIA) PRODUCT #T3046?

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

What is the FDA product code for LYSINE IRON AGAR (LIA) PRODUCT #T3046?

The FDA product code for LYSINE IRON AGAR (LIA) PRODUCT #T3046 is JSH.

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Other records listing Lakewood Biochemical Co., Inc. as applicant

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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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