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FDA 510(k)

TRIPLE SUGAR IRON

K-Number: K842850 · 1984-08-17

ApplicantAnarobe Systems
Decision Date1984-08-17
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRIPLE SUGAR IRON is the device name listed in this FDA 510(k) record. The listed applicant is Anarobe Systems. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842850. 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?

TRIPLE SUGAR IRON is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Anarobe Systems. The 510(k) number is K842850.

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

TRIPLE SUGAR IRON received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842850.

Who is the listed applicant for TRIPLE SUGAR IRON?

The FDA 510(k) record lists Anarobe Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIPLE SUGAR IRON?

The FDA product code for TRIPLE SUGAR IRON is JSH.

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Other records listing Anarobe Systems 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.

K842854MUELLER HINTON BROTHK842851ORNITHINE INDOLE MOTILITYK842852BRAIN HEART INFUSION BROTHK842855CHRISTENSEN'S UREA AGARK842853LYSINE IRON AGARK842849TRYPTICASE SOY BROTH

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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.

K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia 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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