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FDA 510(k)

SLOAN STA-DRI BOOTLEG LEGGING

K-Number: K944276 · 1995-07-31

ApplicantSloan Corp.
Decision Date1995-07-31
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SLOAN STA-DRI BOOTLEG LEGGING is the device name listed in this FDA 510(k) record. The listed applicant is Sloan Corp.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K944276. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLOAN STA-DRI BOOTLEG LEGGING?

SLOAN STA-DRI BOOTLEG LEGGING is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Sloan Corp.. The 510(k) number is K944276.

When did SLOAN STA-DRI BOOTLEG LEGGING receive FDA 510(k) clearance?

SLOAN STA-DRI BOOTLEG LEGGING received FDA 510(k) clearance on 1995-07-31, under 510(k) number K944276.

Who is the listed applicant for SLOAN STA-DRI BOOTLEG LEGGING?

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

What is the FDA product code for SLOAN STA-DRI BOOTLEG LEGGING?

The FDA product code for SLOAN STA-DRI BOOTLEG LEGGING is LYU.

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.

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Other records listing Sloan 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.

K945302SLOAN STA-DRI PANT PROTECTORK944118SLOAN STA-DRI SURGICAL JUMPSUIT

Related Devices (Code: LYU)

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.

K011755STRYKER T4 HYTREL (R) TOGASStryker Corp.K965237NURSES BOUFFANT CAPCopioumed Intl., Inc.K970988FAR-EAST BOUFFANT CAPSFar East Science & Technology Development Co., Ltd.K964364DISPOSABLE APRONInstrument Makar, Inc.K961791DEPUY DISPOSABLE FILTER/HOODDepuy, Inc.K961454AMMI MAGNI-GUARDAmerican Medical Mfg., Inc.

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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