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FDA 510(k)

SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300

K-Number: K873321 · 1987-09-29

ApplicantLakewood Biochemical Co., Inc.
Decision Date1987-09-29
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300 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 1987-09-29 under 510(k) number K873321. 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 SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300?

SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300 is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K873321.

When did SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300 receive FDA 510(k) clearance?

SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300 received FDA 510(k) clearance on 1987-09-29, under 510(k) number K873321.

Who is the listed applicant for SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300?

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 SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300?

The FDA product code for SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300 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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