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FDA 510(k)

EMERGENCY DEPARTMENT LACERATION KIT-

K-Number: K802557 · 1980-11-12

Decision Date1980-11-12
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EMERGENCY DEPARTMENT LACERATION KIT- is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802557. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 206 devices →

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

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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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