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FDA 510(k)

SAWYER FIRST AID KIT

K-Number: K842015 · 1984-07-06

ApplicantSaffeta, Inc.
Decision Date1984-07-06
Product CodeKYP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAWYER FIRST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Saffeta, Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K842015. The device is classified under product code KYP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAWYER FIRST AID KIT?

SAWYER FIRST AID KIT is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Saffeta, Inc.. The 510(k) number is K842015.

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

SAWYER FIRST AID KIT received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842015.

Who is the listed applicant for SAWYER FIRST AID KIT?

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

What is the FDA product code for SAWYER FIRST AID KIT?

The FDA product code for SAWYER FIRST AID KIT is KYP.

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Related Devices (Code: KYP)

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.

K883839ND:YAG LASER SPECTACLES, MST MODEL #YLS-5Marlo Surgical TechnologyK844048DR. HESSEL'S INSECT POISON REMOVERMedie GroupK831312LOPEZ-HORN CARRIERChiron Vision Corp.

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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