MAYFIELD ADULT DISPOSABLE SKULL PIN
K-Number: K923789 · 1993-02-12
Advertisement
Device Summary
Frequently Asked Questions
What is the MAYFIELD ADULT DISPOSABLE SKULL PIN?
MAYFIELD ADULT DISPOSABLE SKULL PIN is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Ohio Medical Instrument Co., Inc.. The 510(k) number is K923789.
When did MAYFIELD ADULT DISPOSABLE SKULL PIN receive FDA 510(k) clearance?
MAYFIELD ADULT DISPOSABLE SKULL PIN received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923789.
Who is the listed applicant for MAYFIELD ADULT DISPOSABLE SKULL PIN?
The FDA 510(k) record lists Ohio Medical Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAYFIELD ADULT DISPOSABLE SKULL PIN?
The FDA product code for MAYFIELD ADULT DISPOSABLE SKULL PIN is HBL.
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.
Other records listing Ohio Medical Instrument Co., Inc. 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.
Related Devices (Code: HBL)
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.
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.
Advertisement