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FDA 510(k)

ALT -LTS

K-Number: K832639 · 1983-09-12

ApplicantElectro-Nucleonics Laboratories, Inc.
Decision Date1983-09-12
Product CodeCKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALT -LTS is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Nucleonics Laboratories, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832639. The device is classified under product code CKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALT -LTS?

ALT -LTS is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Electro-Nucleonics Laboratories, Inc.. The 510(k) number is K832639.

When did ALT -LTS receive FDA 510(k) clearance?

ALT -LTS received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832639.

Who is the listed applicant for ALT -LTS?

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

What is the FDA product code for ALT -LTS?

The FDA product code for ALT -LTS is CKA.

Other records listing Electro-Nucleonics Laboratories, Inc. as applicant

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Related Devices (Code: CKA)

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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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