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FDA 510(k)

LITHIUM DILUENT

K-Number: K830283 · 1983-02-28

ApplicantShaban Mfg. Co.
Decision Date1983-02-28
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LITHIUM DILUENT is the device name listed in this FDA 510(k) record. The listed applicant is Shaban Mfg. Co.. It received FDA 510(k) clearance on 1983-02-28 under 510(k) number K830283. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHIUM DILUENT?

LITHIUM DILUENT is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is Shaban Mfg. Co.. The 510(k) number is K830283.

When did LITHIUM DILUENT receive FDA 510(k) clearance?

LITHIUM DILUENT received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830283.

Who is the listed applicant for LITHIUM DILUENT?

The FDA 510(k) record lists Shaban Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITHIUM DILUENT?

The FDA product code for LITHIUM DILUENT is JIS.

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Other records listing Shaban Mfg. Co. 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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Related Devices (Code: JIS)

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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