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FDA 510(k)

HAND PACK

K-Number: K914934 · 1993-01-21

ApplicantWestmark Hospital Supplies
Decision Date1993-01-21
Product CodeKDO
Advisory CommitteeGU
DecisionUnknown

Device Summary

HAND PACK is the device name listed in this FDA 510(k) record. The listed applicant is Westmark Hospital Supplies. It received FDA 510(k) clearance on 1993-01-21 under 510(k) number K914934. The device is classified under product code KDO. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HAND PACK?

HAND PACK is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Westmark Hospital Supplies. The 510(k) number is K914934.

When did HAND PACK receive FDA 510(k) clearance?

HAND PACK received FDA 510(k) clearance on 1993-01-21, under 510(k) number K914934.

Who is the listed applicant for HAND PACK?

The FDA 510(k) record lists Westmark Hospital Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAND PACK?

The FDA product code for HAND PACK is KDO.

Other records listing Westmark Hospital Supplies 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.

K914928BASIC SET UP TRAYK914935HEART PACK IIK914933HEART PACK IIIK914927DRESSING CHANGE KITK914929LACERATION TRAYK914932SUTURE REMOVAL KIT

View all 7 devices →

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.

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