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FDA 510(k)

XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601

K-Number: K873226 · 1987-09-23

Decision Date1987-09-23
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601 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 1987-09-23 under 510(k) number K873226. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601?

XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601 is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K873226.

When did XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601 receive FDA 510(k) clearance?

XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601 received FDA 510(k) clearance on 1987-09-23, under 510(k) number K873226.

Who is the listed applicant for XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601?

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 XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601?

The FDA product code for XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601 is JSI.

Related Clinical Trials

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.

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.

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Related Devices (Code: JSI)

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.

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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