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FDA 510(k)

AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)

K-Number: K953968 · 1996-02-05

ApplicantAesculap, Inc.
Decision Date1996-02-05
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K953968. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)?

AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Aesculap, Inc.. The 510(k) number is K953968.

When did AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) receive FDA 510(k) clearance?

AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) received FDA 510(k) clearance on 1996-02-05, under 510(k) number K953968.

Who is the listed applicant for AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)?

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

What is the FDA product code for AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON)?

The FDA product code for AESCULAP POWER SYSTEMS (ELAN-E & MICROTRON) is HWE.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: HWE)

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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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