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FDA 510(k)

CODMAN DISPOSABLE SCALP CLIP APPLIER

K-Number: K905433 · 1991-02-21

ApplicantCodman & Shurtleff, Inc.
Decision Date1991-02-21
Product CodeHBO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN DISPOSABLE SCALP CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K905433. The device is classified under product code HBO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN DISPOSABLE SCALP CLIP APPLIER?

CODMAN DISPOSABLE SCALP CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K905433.

When did CODMAN DISPOSABLE SCALP CLIP APPLIER receive FDA 510(k) clearance?

CODMAN DISPOSABLE SCALP CLIP APPLIER received FDA 510(k) clearance on 1991-02-21, under 510(k) number K905433.

Who is the listed applicant for CODMAN DISPOSABLE SCALP CLIP APPLIER?

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

What is the FDA product code for CODMAN DISPOSABLE SCALP CLIP APPLIER?

The FDA product code for CODMAN DISPOSABLE SCALP CLIP APPLIER is HBO.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: HBO)

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.

K253814Raney Clips KitBeijing Honghugaoxiang Science and Technology Development COK050044MEDTRONIC CLIP GUN KITMedtronic NeurosurgeryK033660STORZ RANEY SCALP CLIP, MODEL 1-20-004-05Rudolf Storz GmbHK012219SCALPFIX CLIP SYSTEMAesculap, Inc.K944311ACRA-CUTAcra Cut, Inc.K896723CLIP GUN WITH RANEY TYPE SCALP CLIPSOmni Medical Designs

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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