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FDA 510(k)

MULTI-TITER DISPENSER

K-Number: K832203 · 1983-08-08

ApplicantHamilton Co.
Decision Date1983-08-08
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MULTI-TITER DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Co.. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K832203. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-TITER DISPENSER?

MULTI-TITER DISPENSER is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Hamilton Co.. The 510(k) number is K832203.

When did MULTI-TITER DISPENSER receive FDA 510(k) clearance?

MULTI-TITER DISPENSER received FDA 510(k) clearance on 1983-08-08, under 510(k) number K832203.

Who is the listed applicant for MULTI-TITER DISPENSER?

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

What is the FDA product code for MULTI-TITER DISPENSER?

The FDA product code for MULTI-TITER DISPENSER is JTC.

Related Clinical Trials

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.

Other records listing Hamilton 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.

View all 16 devices →

Related Devices (Code: JTC)

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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