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FDA 510(k)

DOCTOR VELLETTE'S INJECTOR

K-Number: K833426 · 1984-01-13

ApplicantDeproco, Inc.
Decision Date1984-01-13
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DOCTOR VELLETTE'S INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Deproco, Inc.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K833426. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOCTOR VELLETTE'S INJECTOR?

DOCTOR VELLETTE'S INJECTOR is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Deproco, Inc.. The 510(k) number is K833426.

When did DOCTOR VELLETTE'S INJECTOR receive FDA 510(k) clearance?

DOCTOR VELLETTE'S INJECTOR received FDA 510(k) clearance on 1984-01-13, under 510(k) number K833426.

Who is the listed applicant for DOCTOR VELLETTE'S INJECTOR?

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

What is the FDA product code for DOCTOR VELLETTE'S INJECTOR?

The FDA product code for DOCTOR VELLETTE'S INJECTOR is EJI.

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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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