EMERGENCY DEPARTMENT LACERATION KIT-
K-Number: K802557 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the EMERGENCY DEPARTMENT LACERATION KIT-?
EMERGENCY DEPARTMENT LACERATION KIT- is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K802557.
When did EMERGENCY DEPARTMENT LACERATION KIT- receive FDA 510(k) clearance?
EMERGENCY DEPARTMENT LACERATION KIT- received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802557.
Who is the listed applicant for EMERGENCY DEPARTMENT LACERATION KIT-?
The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMERGENCY DEPARTMENT LACERATION KIT-?
The FDA product code for EMERGENCY DEPARTMENT LACERATION KIT- 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 Johnson & Johnson Professionals, 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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