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FDA 510(k)

I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE

K-Number: K852375 · 1985-07-11

Decision Date1985-07-11
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1985-07-11 under 510(k) number K852375. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE?

I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE is a medical device that received FDA 510(k) clearance on 1985-07-11. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K852375.

When did I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE receive FDA 510(k) clearance?

I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE received FDA 510(k) clearance on 1985-07-11, under 510(k) number K852375.

Who is the listed applicant for I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE?

The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE?

The FDA product code for I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE is LRS.

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 Ferris Mfg. 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.

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Related Devices (Code: LRS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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