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FDA 510(k)

P4802 BEA

K-Number: K870339 · 1987-02-13

ApplicantLakewood Biochemical Co., Inc.
Decision Date1987-02-13
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

P4802 BEA 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 K870339. 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 P4802 BEA?

P4802 BEA 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 K870339.

When did P4802 BEA receive FDA 510(k) clearance?

P4802 BEA received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870339.

Who is the listed applicant for P4802 BEA?

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 P4802 BEA?

The FDA product code for P4802 BEA is JSI.

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

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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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia Manufacturers, Inc.

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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