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FDA 510(k)

QUAD PLATE (4 DIFFERENT MEDIA)

K-Number: K874344 · 1987-11-06

Decision Date1987-11-06
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUAD PLATE (4 DIFFERENT MEDIA) 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 1987-11-06 under 510(k) number K874344. 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 QUAD PLATE (4 DIFFERENT MEDIA)?

QUAD PLATE (4 DIFFERENT MEDIA) is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K874344.

When did QUAD PLATE (4 DIFFERENT MEDIA) receive FDA 510(k) clearance?

QUAD PLATE (4 DIFFERENT MEDIA) received FDA 510(k) clearance on 1987-11-06, under 510(k) number K874344.

Who is the listed applicant for QUAD PLATE (4 DIFFERENT MEDIA)?

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 QUAD PLATE (4 DIFFERENT MEDIA)?

The FDA product code for QUAD PLATE (4 DIFFERENT MEDIA) 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.

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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