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FDA 510(k)

HC40/HC75 PREPACKED COLUMS

K-Number: K832198 · 1983-08-12

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

Device Summary

HC40/HC75 PREPACKED COLUMS 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 K832198. The device is classified under product code DJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HC40/HC75 PREPACKED COLUMS?

HC40/HC75 PREPACKED COLUMS 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 K832198.

When did HC40/HC75 PREPACKED COLUMS receive FDA 510(k) clearance?

HC40/HC75 PREPACKED COLUMS received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832198.

Who is the listed applicant for HC40/HC75 PREPACKED COLUMS?

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 PREPACKED COLUMS?

The FDA product code for HC40/HC75 PREPACKED COLUMS is DJY.

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.

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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 →

Related Devices (Code: DJY)

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.

K890113THE CDI(R) SYSTEM 400Cardiovascular Devices, Inc.K883615LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73Supelco, Inc.K881361SOLID PHASE EXTRACTION TUBESSupelco, Inc.K850963DUPONT PREP TYPE SI EXTRACITON CARTRIDGEE.I. Dupont DE Nemours & Co., Inc.K840985TRISACRYL GF 05 & TRISACRYL GF 2000Lkb Instruments, Inc.K831289PREFILLED IEC COLUMNSBerwick Medical Products, Inc.

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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