FDA 510(k)

SHERIDAN/HVT,CF, UNCUFFED

K-Number: K822082 · 1982-08-10

Decision Date1982-08-10

Product CodeBTR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SHERIDAN/HVT,CF, UNCUFFED 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 1982-08-10 under 510(k) number K822082. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERIDAN/HVT,CF, UNCUFFED?

SHERIDAN/HVT,CF, UNCUFFED is a medical device that received FDA 510(k) clearance on 1982-08-10. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K822082.

When did SHERIDAN/HVT,CF, UNCUFFED receive FDA 510(k) clearance?

SHERIDAN/HVT,CF, UNCUFFED received FDA 510(k) clearance on 1982-08-10, under 510(k) number K822082.

Who is the listed applicant for SHERIDAN/HVT,CF, UNCUFFED?

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/HVT,CF, UNCUFFED?

The FDA product code for SHERIDAN/HVT,CF, UNCUFFED is BTR.

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Related Devices (Code: BTR)

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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.