Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SLOAN STA-DRI SURGICAL JUMPSUIT

K-Number: K944118 · 1995-07-31

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

Device Summary

SLOAN STA-DRI SURGICAL JUMPSUIT 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 K944118. 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 SURGICAL JUMPSUIT?

SLOAN STA-DRI SURGICAL JUMPSUIT 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 K944118.

When did SLOAN STA-DRI SURGICAL JUMPSUIT receive FDA 510(k) clearance?

SLOAN STA-DRI SURGICAL JUMPSUIT received FDA 510(k) clearance on 1995-07-31, under 510(k) number K944118.

Who is the listed applicant for SLOAN STA-DRI SURGICAL JUMPSUIT?

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 SURGICAL JUMPSUIT?

The FDA product code for SLOAN STA-DRI SURGICAL JUMPSUIT 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.

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.

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.

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.

↑