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FDA 510(k)

SHERIDAN YSI/SONATEMP

K-Number: K841098 · 1984-04-30

Decision Date1984-04-30
Product CodeBZT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHERIDAN YSI/SONATEMP is the device name listed in this FDA 510(k) record. The listed applicant is Sheridan Catheter Corp.. It received FDA 510(k) clearance on 1984-04-30 under 510(k) number K841098. The device is classified under product code BZT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERIDAN YSI/SONATEMP?

SHERIDAN YSI/SONATEMP is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K841098.

When did SHERIDAN YSI/SONATEMP receive FDA 510(k) clearance?

SHERIDAN YSI/SONATEMP received FDA 510(k) clearance on 1984-04-30, under 510(k) number K841098.

Who is the listed applicant for SHERIDAN YSI/SONATEMP?

The FDA 510(k) record lists Sheridan Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHERIDAN YSI/SONATEMP?

The FDA product code for SHERIDAN YSI/SONATEMP is BZT.

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 Sheridan Catheter Corp. 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.

View all 39 devices →

Related Devices (Code: BZT)

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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