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FDA 510(k)

REDUCT-ASE TUBES

K-Number: K811852 · 1981-07-16

ApplicantMicrochemical Specialities, Co.
Decision Date1981-07-16
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

REDUCT-ASE TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Microchemical Specialities, Co.. It received FDA 510(k) clearance on 1981-07-16 under 510(k) number K811852. 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 REDUCT-ASE TUBES?

REDUCT-ASE TUBES is a medical device that received FDA 510(k) clearance on 1981-07-16. The listed applicant is Microchemical Specialities, Co.. The 510(k) number is K811852.

When did REDUCT-ASE TUBES receive FDA 510(k) clearance?

REDUCT-ASE TUBES received FDA 510(k) clearance on 1981-07-16, under 510(k) number K811852.

Who is the listed applicant for REDUCT-ASE TUBES?

The FDA 510(k) record lists Microchemical Specialities, Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REDUCT-ASE TUBES?

The FDA product code for REDUCT-ASE TUBES is JSH.

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Other records listing Microchemical Specialities, Co. 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.

K823198RAPID PRESUMPTIVE IDENT. GPA STREPK821992ALPHA-TOXIN DISCSK811853PHOLPHORYL-ASE TUBESK811854GALACTOSID-ASE TUBESK801915ENZYME-ASE I TUBESK801916ORNITH-ASE TUBES

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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.

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