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FDA 510(k)

FIRST AID KIT(S)

K-Number: K963298 · 1996-11-06

ApplicantVector, Inc.
Decision Date1996-11-06
Product CodeBYG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FIRST AID KIT(S) is the device name listed in this FDA 510(k) record. The listed applicant is Vector, Inc.. It received FDA 510(k) clearance on 1996-11-06 under 510(k) number K963298. The device is classified under product code BYG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST AID KIT(S)?

FIRST AID KIT(S) is a medical device that received FDA 510(k) clearance on 1996-11-06. The listed applicant is Vector, Inc.. The 510(k) number is K963298.

When did FIRST AID KIT(S) receive FDA 510(k) clearance?

FIRST AID KIT(S) received FDA 510(k) clearance on 1996-11-06, under 510(k) number K963298.

Who is the listed applicant for FIRST AID KIT(S)?

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

What is the FDA product code for FIRST AID KIT(S)?

The FDA product code for FIRST AID KIT(S) is BYG.

Related Clinical Trials

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Related Devices (Code: BYG)

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.

K962848HANS RUDOLPH NASAL CPAP MASKHans Rudolph, Inc.K945482DISPOSABLE, CPAP OXYGEN MASKFvtnksK953464WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASKWestmed, Inc.K953039VARIOUS ADULT & CHILD HIGH CON/NONREBREATH OXY MASKSDadsun Corp., Ltd.K945472WESTMED PEDIATRIC AND ADULT AEROSOL MASKWestmed Intl.K942907JEMSDAL MASKRespan Products, Inc.

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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