DENTAL SURGICAL WRAP #3007 A,B,C
K-Number: K891214 · 1989-04-14
Advertisement
Device Summary
Frequently Asked Questions
What is the DENTAL SURGICAL WRAP #3007 A,B,C?
DENTAL SURGICAL WRAP #3007 A,B,C is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is Pro-Safe Professional Linens, Inc.. The 510(k) number is K891214.
When did DENTAL SURGICAL WRAP #3007 A,B,C receive FDA 510(k) clearance?
DENTAL SURGICAL WRAP #3007 A,B,C received FDA 510(k) clearance on 1989-04-14, under 510(k) number K891214.
Who is the listed applicant for DENTAL SURGICAL WRAP #3007 A,B,C?
The FDA 510(k) record lists Pro-Safe Professional Linens, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL SURGICAL WRAP #3007 A,B,C?
The FDA product code for DENTAL SURGICAL WRAP #3007 A,B,C is KCT.
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 Pro-Safe Professional Linens, 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: KCT)
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.
Advertisement