FDA 510(k)

DECARBOXYLASE MOELLER BASE WITH OR WITH-

K-Number: K792425 · 1979-12-27

ApplicantIsle Media and Sterile Products, Inc.

Decision Date1979-12-27

Product CodeJSE

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

DECARBOXYLASE MOELLER BASE WITH OR WITH- is the device name listed in this FDA 510(k) record. The listed applicant is Isle Media and Sterile Products, Inc.. It received FDA 510(k) clearance on 1979-12-27 under 510(k) number K792425. 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 DECARBOXYLASE MOELLER BASE WITH OR WITH-?

DECARBOXYLASE MOELLER BASE WITH OR WITH- is a medical device that received FDA 510(k) clearance on 1979-12-27. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K792425.

When did DECARBOXYLASE MOELLER BASE WITH OR WITH- receive FDA 510(k) clearance?

DECARBOXYLASE MOELLER BASE WITH OR WITH- received FDA 510(k) clearance on 1979-12-27, under 510(k) number K792425.

Who is the listed applicant for DECARBOXYLASE MOELLER BASE WITH OR WITH-?

The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DECARBOXYLASE MOELLER BASE WITH OR WITH-?

The FDA product code for DECARBOXYLASE MOELLER BASE WITH OR WITH- is JSE.

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Other records listing Isle Media and Sterile Products, Inc. as applicant

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Related Devices (Code: JSE)

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy Media K880116MRVP BROTHHardy Media K874537KLIGLER 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.