ALLRAP/SLIP-N-GRIP
K-Number: K960352 · 1996-02-21
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Device Summary
Frequently Asked Questions
What is the ALLRAP/SLIP-N-GRIP?
ALLRAP/SLIP-N-GRIP is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is Dental Disposables Intl., Inc.. The 510(k) number is K960352.
When did ALLRAP/SLIP-N-GRIP receive FDA 510(k) clearance?
ALLRAP/SLIP-N-GRIP received FDA 510(k) clearance on 1996-02-21, under 510(k) number K960352.
Who is the listed applicant for ALLRAP/SLIP-N-GRIP?
The FDA 510(k) record lists Dental Disposables Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLRAP/SLIP-N-GRIP?
The FDA product code for ALLRAP/SLIP-N-GRIP is EFB.
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.
Related Devices (Code: EFB)
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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