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FDA 510(k)

SHILEY DISPOS. TEMP. PROBES

K-Number: K833981 · 1984-03-27

ApplicantShiley, Inc.
Decision Date1984-03-27
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHILEY DISPOS. TEMP. PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1984-03-27 under 510(k) number K833981. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHILEY DISPOS. TEMP. PROBES?

SHILEY DISPOS. TEMP. PROBES is a medical device that received FDA 510(k) clearance on 1984-03-27. The listed applicant is Shiley, Inc.. The 510(k) number is K833981.

When did SHILEY DISPOS. TEMP. PROBES receive FDA 510(k) clearance?

SHILEY DISPOS. TEMP. PROBES received FDA 510(k) clearance on 1984-03-27, under 510(k) number K833981.

Who is the listed applicant for SHILEY DISPOS. TEMP. PROBES?

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 SHILEY DISPOS. TEMP. PROBES?

The FDA product code for SHILEY DISPOS. TEMP. PROBES is FLL.

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.

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Related Devices (Code: FLL)

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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