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FDA 510(k)

LECITHIN LACTOSE AGAR

K-Number: K823072 · 1982-11-05

ApplicantGranite Diagnostics, Inc.
Decision Date1982-11-05
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LECITHIN LACTOSE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K823072. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LECITHIN LACTOSE AGAR?

LECITHIN LACTOSE AGAR is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K823072.

When did LECITHIN LACTOSE AGAR receive FDA 510(k) clearance?

LECITHIN LACTOSE AGAR received FDA 510(k) clearance on 1982-11-05, under 510(k) number K823072.

Who is the listed applicant for LECITHIN LACTOSE AGAR?

The FDA 510(k) record lists Granite Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LECITHIN LACTOSE AGAR?

The FDA product code for LECITHIN LACTOSE AGAR is JSE.

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Related Devices (Code: JSE)

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.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., 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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