HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS
K-Number: K884395 · 1989-01-10
Advertisement
Device Summary
Frequently Asked Questions
What is the HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS?
HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS is a medical device that received FDA 510(k) clearance on 1989-01-10. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K884395.
When did HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS receive FDA 510(k) clearance?
HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS received FDA 510(k) clearance on 1989-01-10, under 510(k) number K884395.
Who is the listed applicant for HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS?
The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS?
The FDA product code for HP 21362B TRANSESOPHAGEAL ULTRASOUND IMAGING TRANS is IYO.
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 Hewlett-Packard Co. 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: IYO)
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