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)

CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL-

K-Number: K844920 · 1985-04-01

Decision Date1985-04-01
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL- is the device name listed in this FDA 510(k) record. The listed applicant is Papeteries Depont-Audemer. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K844920. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL-?

CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL- is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Papeteries Depont-Audemer. The 510(k) number is K844920.

When did CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL- receive FDA 510(k) clearance?

CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL- received FDA 510(k) clearance on 1985-04-01, under 510(k) number K844920.

Who is the listed applicant for CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL-?

The FDA 510(k) record lists Papeteries Depont-Audemer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL-?

The FDA product code for CSR WRAP - CENTRAL SUPPLY ROOM WRAP FOR STERIL- is FRG.

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.

Related Devices (Code: FRG)

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.

↑