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)

ACCU-SORB STERILE STOCKINETTES

K-Number: K791070 · 1979-06-20

Decision Date1979-06-20
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACCU-SORB STERILE STOCKINETTES is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1979-06-20 under 510(k) number K791070. 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 ACCU-SORB STERILE STOCKINETTES?

ACCU-SORB STERILE STOCKINETTES is a medical device that received FDA 510(k) clearance on 1979-06-20. The listed applicant is Medline Industries, Inc.. The 510(k) number is K791070.

When did ACCU-SORB STERILE STOCKINETTES receive FDA 510(k) clearance?

ACCU-SORB STERILE STOCKINETTES received FDA 510(k) clearance on 1979-06-20, under 510(k) number K791070.

Who is the listed applicant for ACCU-SORB STERILE STOCKINETTES?

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

What is the FDA product code for ACCU-SORB STERILE STOCKINETTES?

The FDA product code for ACCU-SORB STERILE STOCKINETTES 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 Medline Industries, 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 223 devices →

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.

↑