HEMO-O-LOK
K-Number: K941972 · 1994-06-29
Advertisement
Device Summary
Frequently Asked Questions
What is the HEMO-O-LOK?
HEMO-O-LOK is a medical device that received FDA 510(k) clearance on 1994-06-29. The listed applicant is King & Spalding. The 510(k) number is K941972.
When did HEMO-O-LOK receive FDA 510(k) clearance?
HEMO-O-LOK received FDA 510(k) clearance on 1994-06-29, under 510(k) number K941972.
Who is the listed applicant for HEMO-O-LOK?
The FDA 510(k) record lists King & Spalding as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMO-O-LOK?
The FDA product code for HEMO-O-LOK is FZP.
Other records listing King & Spalding 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: FZP)
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