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FDA 510(k)

AMES TDA NETILMICIN TEST & SERUM

K-Number: K832088 · 1983-10-28

ApplicantMiles Laboratories, Inc.
Decision Date1983-10-28
Product CodeLCE
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

AMES TDA NETILMICIN TEST & SERUM 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 1983-10-28 under 510(k) number K832088. The device is classified under product code LCE. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMES TDA NETILMICIN TEST & SERUM?

AMES TDA NETILMICIN TEST & SERUM is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K832088.

When did AMES TDA NETILMICIN TEST & SERUM receive FDA 510(k) clearance?

AMES TDA NETILMICIN TEST & SERUM received FDA 510(k) clearance on 1983-10-28, under 510(k) number K832088.

Who is the listed applicant for AMES TDA NETILMICIN TEST & SERUM?

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 AMES TDA NETILMICIN TEST & SERUM?

The FDA product code for AMES TDA NETILMICIN TEST & SERUM is LCE.

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Related Devices (Code: LCE)

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

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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