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FDA 510(k)

DTM AGAR

K-Number: K840519 · 1984-02-27

ApplicantScientific Device Laboratory, Inc.
Decision Date1984-02-27
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DTM AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Device Laboratory, Inc.. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K840519. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DTM AGAR?

DTM AGAR is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Scientific Device Laboratory, Inc.. The 510(k) number is K840519.

When did DTM AGAR receive FDA 510(k) clearance?

DTM AGAR received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840519.

Who is the listed applicant for DTM AGAR?

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

What is the FDA product code for DTM AGAR?

The FDA product code for DTM AGAR is JSJ.

Other records listing Scientific Device Laboratory, Inc. as applicant

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Related Devices (Code: JSJ)

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.

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia 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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