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FDA 510(k)

9-WAY URINE TEST WITH ASCORBIC

K-Number: K771755 · 1977-10-25

ApplicantMiles Laboratories, Inc.
Decision Date1977-10-25
Product CodeJIL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

9-WAY URINE TEST WITH ASCORBIC is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771755. The device is classified under product code JIL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 9-WAY URINE TEST WITH ASCORBIC?

9-WAY URINE TEST WITH ASCORBIC is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K771755.

When did 9-WAY URINE TEST WITH ASCORBIC receive FDA 510(k) clearance?

9-WAY URINE TEST WITH ASCORBIC received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771755.

Who is the listed applicant for 9-WAY URINE TEST WITH ASCORBIC?

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

What is the FDA product code for 9-WAY URINE TEST WITH ASCORBIC?

The FDA product code for 9-WAY URINE TEST WITH ASCORBIC is JIL.

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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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