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)

Bodygard SFS Surgical Gown Level 3

K-Number: K202845 · 2022-02-24

Decision Date2022-02-24
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Bodygard SFS Surgical Gown Level 3 is the device name listed in this FDA 510(k) record. The listed applicant is Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi. It received FDA 510(k) clearance on 2022-02-24 under 510(k) number K202845. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bodygard SFS Surgical Gown Level 3?

Bodygard SFS Surgical Gown Level 3 is a medical device that received FDA 510(k) clearance on 2022-02-24. The listed applicant is Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi. The 510(k) number is K202845.

When did Bodygard SFS Surgical Gown Level 3 receive FDA 510(k) clearance?

Bodygard SFS Surgical Gown Level 3 received FDA 510(k) clearance on 2022-02-24, under 510(k) number K202845.

Who is the listed applicant for Bodygard SFS Surgical Gown Level 3?

The FDA 510(k) record lists Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bodygard SFS Surgical Gown Level 3?

The FDA product code for Bodygard SFS Surgical Gown Level 3 is FYA.

Other records listing Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi 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: FYA)

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.