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FDA 510(k)

PRP-1 REVERSED PHASE RESIN

K-Number: K832197 · 1983-08-12

ApplicantHamilton Co.
Decision Date1983-08-12
Product CodeDMZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRP-1 REVERSED PHASE 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 1983-08-12 under 510(k) number K832197. The device is classified under product code DMZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRP-1 REVERSED PHASE RESIN?

PRP-1 REVERSED PHASE RESIN is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Hamilton Co.. The 510(k) number is K832197.

When did PRP-1 REVERSED PHASE RESIN receive FDA 510(k) clearance?

PRP-1 REVERSED PHASE RESIN received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832197.

Who is the listed applicant for PRP-1 REVERSED PHASE 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 PRP-1 REVERSED PHASE RESIN?

The FDA product code for PRP-1 REVERSED PHASE RESIN is DMZ.

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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

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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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