H-H SUBGALEAL TROCAR
K-Number: K865075 · 1987-01-13
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Device Summary
Frequently Asked Questions
What is the H-H SUBGALEAL TROCAR?
H-H SUBGALEAL TROCAR is a medical device that received FDA 510(k) clearance on 1987-01-13. The listed applicant is Holter-Hausner Intl.. The 510(k) number is K865075.
When did H-H SUBGALEAL TROCAR receive FDA 510(k) clearance?
H-H SUBGALEAL TROCAR received FDA 510(k) clearance on 1987-01-13, under 510(k) number K865075.
Who is the listed applicant for H-H SUBGALEAL TROCAR?
The FDA 510(k) record lists Holter-Hausner Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for H-H SUBGALEAL TROCAR?
The FDA product code for H-H SUBGALEAL TROCAR is GYK.
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 Holter-Hausner Intl. 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: GYK)
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.
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