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FDA 510(k)

TRIPLE SUGAR IRON AGAR

K-Number: K851597 · 1985-05-13

Decision Date1985-05-13
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRIPLE SUGAR IRON AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Micro-Media. It received FDA 510(k) clearance on 1985-05-13 under 510(k) number K851597. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPLE SUGAR IRON AGAR?

TRIPLE SUGAR IRON AGAR is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is Preferred Micro-Media. The 510(k) number is K851597.

When did TRIPLE SUGAR IRON AGAR receive FDA 510(k) clearance?

TRIPLE SUGAR IRON AGAR received FDA 510(k) clearance on 1985-05-13, under 510(k) number K851597.

Who is the listed applicant for TRIPLE SUGAR IRON AGAR?

The FDA 510(k) record lists Preferred Micro-Media as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIPLE SUGAR IRON AGAR?

The FDA product code for TRIPLE SUGAR IRON AGAR is JSH.

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 Preferred Micro-Media 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 28 devices →

Related Devices (Code: JSH)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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