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FDA 510(k)

INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515

K-Number: K892944 · 1989-07-19

Decision Date1989-07-19
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515 is the device name listed in this FDA 510(k) record. The listed applicant is Interspec, Inc.. It received FDA 510(k) clearance on 1989-07-19 under 510(k) number K892944. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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