FIRST AID KITS
K-Number: K831795 · 1983-09-01
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Device Summary
Frequently Asked Questions
What is the FIRST AID KITS?
FIRST AID KITS is a medical device that received FDA 510(k) clearance on 1983-09-01. The listed applicant is I M, Inc.. The 510(k) number is K831795.
When did FIRST AID KITS receive FDA 510(k) clearance?
FIRST AID KITS received FDA 510(k) clearance on 1983-09-01, under 510(k) number K831795.
Who is the listed applicant for FIRST AID KITS?
The FDA 510(k) record lists I M, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIRST AID KITS?
The FDA product code for FIRST AID KITS is KDD.
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 I M, 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.
Related Devices (Code: KDD)
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
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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