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FDA 510(k)

P1012 BE AGAR

K-Number: K870341 · 1987-02-13

Decision Date1987-02-13
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

P1012 BE AGAR 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 1987-02-13 under 510(k) number K870341. 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 P1012 BE AGAR?

P1012 BE AGAR is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K870341.

When did P1012 BE AGAR receive FDA 510(k) clearance?

P1012 BE AGAR received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870341.

Who is the listed applicant for P1012 BE AGAR?

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 P1012 BE AGAR?

The FDA product code for P1012 BE AGAR is JSI.

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.

View all 89 devices →

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

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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