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)

DISPOSABLE SURGICAL TOWEL (NON-STERILE)

K-Number: K905005 · 1990-12-11

Decision Date1990-12-11
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SURGICAL TOWEL (NON-STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Marand Products, Inc.. It received FDA 510(k) clearance on 1990-12-11 under 510(k) number K905005. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SURGICAL TOWEL (NON-STERILE)?

DISPOSABLE SURGICAL TOWEL (NON-STERILE) is a medical device that received FDA 510(k) clearance on 1990-12-11. The listed applicant is Marand Products, Inc.. The 510(k) number is K905005.

When did DISPOSABLE SURGICAL TOWEL (NON-STERILE) receive FDA 510(k) clearance?

DISPOSABLE SURGICAL TOWEL (NON-STERILE) received FDA 510(k) clearance on 1990-12-11, under 510(k) number K905005.

Who is the listed applicant for DISPOSABLE SURGICAL TOWEL (NON-STERILE)?

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

What is the FDA product code for DISPOSABLE SURGICAL TOWEL (NON-STERILE)?

The FDA product code for DISPOSABLE SURGICAL TOWEL (NON-STERILE) is KKX.

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 Marand Products, 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.

Related Devices (Code: KKX)

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.

↑