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FDA 510(k)

PRESTYL JET INJECTOR

K-Number: K922683 · 1994-04-11

ApplicantBma Technologies S.A.
Decision Date1994-04-11
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRESTYL JET INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Bma Technologies S.A.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K922683. 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 PRESTYL JET INJECTOR?

PRESTYL JET INJECTOR is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Bma Technologies S.A.. The 510(k) number is K922683.

When did PRESTYL JET INJECTOR receive FDA 510(k) clearance?

PRESTYL JET INJECTOR received FDA 510(k) clearance on 1994-04-11, under 510(k) number K922683.

Who is the listed applicant for PRESTYL JET INJECTOR?

The FDA 510(k) record lists Bma Technologies S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESTYL JET INJECTOR?

The FDA product code for PRESTYL JET INJECTOR is EJI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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