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FDA 510(k)

CODMAN RF-12 DISPOSABLE SCALP CLIP APPLIER

K-Number: K894778 · 1989-12-06

ApplicantCodman & Shurtleff, Inc.
Decision Date1989-12-06
Product CodeHBO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN RF-12 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 1989-12-06 under 510(k) number K894778. 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 RF-12 DISPOSABLE SCALP CLIP APPLIER?

CODMAN RF-12 DISPOSABLE SCALP CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1989-12-06. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K894778.

When did CODMAN RF-12 DISPOSABLE SCALP CLIP APPLIER receive FDA 510(k) clearance?

CODMAN RF-12 DISPOSABLE SCALP CLIP APPLIER received FDA 510(k) clearance on 1989-12-06, under 510(k) number K894778.

Who is the listed applicant for CODMAN RF-12 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 RF-12 DISPOSABLE SCALP CLIP APPLIER?

The FDA product code for CODMAN RF-12 DISPOSABLE SCALP CLIP APPLIER is HBO.

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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.K905433CODMAN DISPOSABLE SCALP CLIP APPLIERCodman & Shurtleff, Inc.

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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