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FDA 510(k)

SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR

K-Number: K862467 · 1986-08-11

ApplicantShiley, Inc.
Decision Date1986-08-11
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1986-08-11 under 510(k) number K862467. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR?

SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR is a medical device that received FDA 510(k) clearance on 1986-08-11. The listed applicant is Shiley, Inc.. The 510(k) number is K862467.

When did SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR receive FDA 510(k) clearance?

SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR received FDA 510(k) clearance on 1986-08-11, under 510(k) number K862467.

Who is the listed applicant for SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR?

The FDA 510(k) record lists Shiley, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR?

The FDA product code for SCHNEIDER-SHILEY SELDINGER INITIAL PUNCTURE INSTR is LIT.

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 Shiley, 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.

View all 174 devices →

Related Devices (Code: LIT)

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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