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FDA 510(k)

PICC WAND PEELABLE SAFETY INTRODUCER

K-Number: K101150 · 2010-08-13

Decision Date2010-08-13
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PICC WAND PEELABLE SAFETY INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Access Scientific, Inc.. It received FDA 510(k) clearance on 2010-08-13 under 510(k) number K101150. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PICC WAND PEELABLE SAFETY INTRODUCER?

PICC WAND PEELABLE SAFETY INTRODUCER is a medical device that received FDA 510(k) clearance on 2010-08-13. The listed applicant is Access Scientific, Inc.. The 510(k) number is K101150.

When did PICC WAND PEELABLE SAFETY INTRODUCER receive FDA 510(k) clearance?

PICC WAND PEELABLE SAFETY INTRODUCER received FDA 510(k) clearance on 2010-08-13, under 510(k) number K101150.

Who is the listed applicant for PICC WAND PEELABLE SAFETY INTRODUCER?

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

What is the FDA product code for PICC WAND PEELABLE SAFETY INTRODUCER?

The FDA product code for PICC WAND PEELABLE SAFETY INTRODUCER is DYB.

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 Access Scientific, 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 8 devices →

Related Devices (Code: DYB)

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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