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FDA 510(k)

ACKERMANN SURGICAL INSTRUMENTS

K-Number: K974382 · 1998-04-21

ApplicantAckermann Instrumente GmbH
Decision Date1998-04-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACKERMANN SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Ackermann Instrumente GmbH. It received FDA 510(k) clearance on 1998-04-21 under 510(k) number K974382. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACKERMANN SURGICAL INSTRUMENTS?

ACKERMANN SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1998-04-21. The listed applicant is Ackermann Instrumente GmbH. The 510(k) number is K974382.

When did ACKERMANN SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

ACKERMANN SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1998-04-21, under 510(k) number K974382.

Who is the listed applicant for ACKERMANN SURGICAL INSTRUMENTS?

The FDA 510(k) record lists Ackermann Instrumente GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACKERMANN SURGICAL INSTRUMENTS?

The FDA product code for ACKERMANN SURGICAL INSTRUMENTS is GCJ.

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Other records listing Ackermann Instrumente GmbH 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.

K111930ACKERMANN EUROPCLIP

Related Devices (Code: GCJ)

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

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