INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515
K-Number: K892944 · 1989-07-19
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Device Summary
Frequently Asked Questions
What is the INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515?
INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 is a medical device that received FDA 510(k) clearance on 1989-07-19. The listed applicant is Interspec, Inc.. The 510(k) number is K892944.
When did INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 receive FDA 510(k) clearance?
INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 received FDA 510(k) clearance on 1989-07-19, under 510(k) number K892944.
Who is the listed applicant for INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515?
The FDA 510(k) record lists Interspec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515?
The FDA product code for INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 is JOP.
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 Interspec, 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: JOP)
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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