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FDA 510(k)

CALIBRATORS, CARBON DIOXIDE

K-Number: K780295 · 1978-04-05

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1978-04-05
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALIBRATORS, CARBON DIOXIDE 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 1978-04-05 under 510(k) number K780295. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALIBRATORS, CARBON DIOXIDE?

CALIBRATORS, CARBON DIOXIDE is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K780295.

When did CALIBRATORS, CARBON DIOXIDE receive FDA 510(k) clearance?

CALIBRATORS, CARBON DIOXIDE received FDA 510(k) clearance on 1978-04-05, under 510(k) number K780295.

Who is the listed applicant for CALIBRATORS, CARBON DIOXIDE?

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 CALIBRATORS, CARBON DIOXIDE?

The FDA product code for CALIBRATORS, CARBON DIOXIDE is JIT.

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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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