FDA 510(k)

AT33 EMG

K-Number: K930578 · 1995-05-19

Decision Date1995-05-19

Product CodeHCC

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

AT33 EMG is the device name listed in this FDA 510(k) record. The listed applicant is Autoject Systems, Inc.. It received FDA 510(k) clearance on 1995-05-19 under 510(k) number K930578. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AT33 EMG?

AT33 EMG is a medical device that received FDA 510(k) clearance on 1995-05-19. The listed applicant is Autoject Systems, Inc.. The 510(k) number is K930578.

When did AT33 EMG receive FDA 510(k) clearance?

AT33 EMG received FDA 510(k) clearance on 1995-05-19, under 510(k) number K930578.

Who is the listed applicant for AT33 EMG?

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

What is the FDA product code for AT33 EMG?

The FDA product code for AT33 EMG is HCC.

Other records listing Autoject Systems, 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.

K930577AT64 SCR K930576AT42 K853031JECT-AID

Related Devices (Code: HCC)

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, LLC

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.