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FDA 510(k)

HC40/HC75 CATION EXCHANGE RESIN

K-Number: K832199 · 1983-08-16

ApplicantHamilton Co.
Decision Date1983-08-16
Product CodeDNH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HC40/HC75 CATION EXCHANGE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Co.. It received FDA 510(k) clearance on 1983-08-16 under 510(k) number K832199. The device is classified under product code DNH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HC40/HC75 CATION EXCHANGE RESIN?

HC40/HC75 CATION EXCHANGE RESIN is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Hamilton Co.. The 510(k) number is K832199.

When did HC40/HC75 CATION EXCHANGE RESIN receive FDA 510(k) clearance?

HC40/HC75 CATION EXCHANGE RESIN received FDA 510(k) clearance on 1983-08-16, under 510(k) number K832199.

Who is the listed applicant for HC40/HC75 CATION EXCHANGE RESIN?

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 HC40/HC75 CATION EXCHANGE RESIN?

The FDA product code for HC40/HC75 CATION EXCHANGE RESIN is DNH.

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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.

K961896MICROLAB 4000, MICROLAB 4200K943493DISCRETE PHOTOMETRIC CHEMISTRY ANALYZERK892369MULTI-PROBE HEAD PLUSK873893LUMICONK871945MICROLAB ATK832205PRECISION LIQUID DISPENSER

View all 16 devices →

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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