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FDA 510(k)

URINE MONOVETTE BORIC ACID

K-Number: K024237 · 2003-04-14

ApplicantSarstedt, Inc.
Decision Date2003-04-14
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

URINE MONOVETTE BORIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Sarstedt, Inc.. It received FDA 510(k) clearance on 2003-04-14 under 510(k) number K024237. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINE MONOVETTE BORIC ACID?

URINE MONOVETTE BORIC ACID is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Sarstedt, Inc.. The 510(k) number is K024237.

When did URINE MONOVETTE BORIC ACID receive FDA 510(k) clearance?

URINE MONOVETTE BORIC ACID received FDA 510(k) clearance on 2003-04-14, under 510(k) number K024237.

Who is the listed applicant for URINE MONOVETTE BORIC ACID?

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

What is the FDA product code for URINE MONOVETTE BORIC ACID?

The FDA product code for URINE MONOVETTE BORIC ACID is JSM.

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Other records listing Sarstedt, Inc. 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.

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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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