FDA 510(k)

ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER

K-Number: K884139 · 1988-10-06

Decision Date1988-10-06

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Safety Products, Inc.. It received FDA 510(k) clearance on 1988-10-06 under 510(k) number K884139. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER?

ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER is a medical device that received FDA 510(k) clearance on 1988-10-06. The listed applicant is Medical Safety Products, Inc.. The 510(k) number is K884139.

When did ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER receive FDA 510(k) clearance?

ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER received FDA 510(k) clearance on 1988-10-06, under 510(k) number K884139.

Who is the listed applicant for ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER?

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

What is the FDA product code for ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER?

The FDA product code for ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER is FMI.

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Other records listing Medical Safety Products, Inc. as applicant

K942624LOK-ON NEEDLE DISPOSAL CONTAINER K913329V-ACCI-GUARD(TM) REUSABLE HOLDER K895075ACCI-GUARD REUSABLE HOLDER K890751ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT K881654ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE

Related Devices (Code: FMI)

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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.