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FDA 510(k)

TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405

K-Number: K873061 · 1987-08-24

ApplicantLakewood Biochemical Co., Inc.
Decision Date1987-08-24
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405 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 1987-08-24 under 510(k) number K873061. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405?

TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405 is a medical device that received FDA 510(k) clearance on 1987-08-24. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K873061.

When did TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405 receive FDA 510(k) clearance?

TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405 received FDA 510(k) clearance on 1987-08-24, under 510(k) number K873061.

Who is the listed applicant for TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405?

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 TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405?

The FDA product code for TRYPTIC SOY AGAR W/5% SHEEP BLOOD - #T1405 is KZI.

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Other records listing Lakewood Biochemical Co., 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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007K882351MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860K880947NUTRIENT AGAR PLATE, SLANT TUBE AND BROTH TUBE

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Related Devices (Code: KZI)

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.

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880122MIDDLEBROOK 7H9 BROTHHardy MediaK880131LOWENSTEIN-JENSEN, GRUFTHardy MediaK880134MIDDLEBROOK 7H11 AGARHardy MediaK880138WALLENSTEIN MEDIUM SLANTHardy Media

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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