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FDA 510(k)

FAST URIC ACID

K-Number: K870632 · 1987-03-13

ApplicantSclavo, Inc.
Decision Date1987-03-13
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FAST URIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Sclavo, Inc.. It received FDA 510(k) clearance on 1987-03-13 under 510(k) number K870632. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAST URIC ACID?

FAST URIC ACID is a medical device that received FDA 510(k) clearance on 1987-03-13. The listed applicant is Sclavo, Inc.. The 510(k) number is K870632.

When did FAST URIC ACID receive FDA 510(k) clearance?

FAST URIC ACID received FDA 510(k) clearance on 1987-03-13, under 510(k) number K870632.

Who is the listed applicant for FAST URIC ACID?

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

What is the FDA product code for FAST URIC ACID?

The FDA product code for FAST URIC ACID is KNK.

Other records listing Sclavo, 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.

View all 82 devices →

Related Devices (Code: KNK)

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

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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