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FDA 510(k)

ALLRAP/SLIP-N-GRIP

K-Number: K960352 · 1996-02-21

Decision Date1996-02-21
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALLRAP/SLIP-N-GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Dental Disposables Intl., Inc.. It received FDA 510(k) clearance on 1996-02-21 under 510(k) number K960352. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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