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FDA 510(k)

CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100

K-Number: K863423 · 1986-09-16

ApplicantPlastic Injectors, Inc.
Decision Date1986-09-16
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100 is the device name listed in this FDA 510(k) record. The listed applicant is Plastic Injectors, Inc.. It received FDA 510(k) clearance on 1986-09-16 under 510(k) number K863423. 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 CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100?

CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100 is a medical device that received FDA 510(k) clearance on 1986-09-16. The listed applicant is Plastic Injectors, Inc.. The 510(k) number is K863423.

When did CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100 receive FDA 510(k) clearance?

CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100 received FDA 510(k) clearance on 1986-09-16, under 510(k) number K863423.

Who is the listed applicant for CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100?

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

What is the FDA product code for CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100?

The FDA product code for CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100 is JTC.

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Other records listing Plastic Injectors, 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.

K884781OPTI-POINTK863374CODE-A-WELL SERIES 1-600, 1-625K844058CODE-A-WALL SERIES 1-250 INOCULUM TRAYK842848CODE-A-WELL 350 MICROTITRATION STRIPSK841632CODE-A-WELL SERIES 200 PLATEK841937CODE-A-WELL SERIES 300 PLATE

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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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.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.

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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