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FDA 510(k)

FILTERMATE UNIVERSAL HARVESTER

K-Number: K924907 · 1992-12-01

ApplicantPackard Instrument Co., Inc.
Decision Date1992-12-01
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FILTERMATE UNIVERSAL HARVESTER is the device name listed in this FDA 510(k) record. The listed applicant is Packard Instrument Co., Inc.. It received FDA 510(k) clearance on 1992-12-01 under 510(k) number K924907. 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 FILTERMATE UNIVERSAL HARVESTER?

FILTERMATE UNIVERSAL HARVESTER is a medical device that received FDA 510(k) clearance on 1992-12-01. The listed applicant is Packard Instrument Co., Inc.. The 510(k) number is K924907.

When did FILTERMATE UNIVERSAL HARVESTER receive FDA 510(k) clearance?

FILTERMATE UNIVERSAL HARVESTER received FDA 510(k) clearance on 1992-12-01, under 510(k) number K924907.

Who is the listed applicant for FILTERMATE UNIVERSAL HARVESTER?

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

What is the FDA product code for FILTERMATE UNIVERSAL HARVESTER?

The FDA product code for FILTERMATE UNIVERSAL HARVESTER 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.

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Other records listing Packard Instrument Co., Inc. 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.

K913664ROSYS MODELS 100 AND 200K901808MICROMATE 196 MODEL A961960K883749PROBE(TM) MODELS 700 AND 1000

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.

K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.K891768GENETIC SYSTEMS MICROPLATE WASHERGenetic Systems Corp.

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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