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FDA 510(k)

ACCULUPE

K-Number: K955184 · 1996-01-24

ApplicantE For M Imaging Systems Div., Marquette Electronic
Decision Date1996-01-24
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCULUPE is the device name listed in this FDA 510(k) record. The listed applicant is E For M Imaging Systems Div., Marquette Electronic. It received FDA 510(k) clearance on 1996-01-24 under 510(k) number K955184. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCULUPE?

ACCULUPE is a medical device that received FDA 510(k) clearance on 1996-01-24. The listed applicant is E For M Imaging Systems Div., Marquette Electronic. The 510(k) number is K955184.

When did ACCULUPE receive FDA 510(k) clearance?

ACCULUPE received FDA 510(k) clearance on 1996-01-24, under 510(k) number K955184.

Who is the listed applicant for ACCULUPE?

The FDA 510(k) record lists E For M Imaging Systems Div., Marquette Electronic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCULUPE?

The FDA product code for ACCULUPE is LMB.

Related Clinical Trials

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.

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Other records listing E For M Imaging Systems Div., Marquette Electronic 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.

K974504EPS

Related Devices (Code: LMB)

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.

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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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