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FDA 510(k)

METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM

K-Number: K862359 · 1986-08-19

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1986-08-19
Product CodeCIG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1986-08-19 under 510(k) number K862359. The device is classified under product code CIG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM?

METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM is a medical device that received FDA 510(k) clearance on 1986-08-19. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K862359.

When did METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM receive FDA 510(k) clearance?

METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM received FDA 510(k) clearance on 1986-08-19, under 510(k) number K862359.

Who is the listed applicant for METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM?

The FDA product code for METH./CALI./INTRU. CHECK FOR THE DIMENSION SYSTEM is CIG.

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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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