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FDA 510(k)

ACE BASIC DENTAL IMPLANT PACK II

K-Number: K922649 · 1994-01-10

Decision Date1994-01-10
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACE BASIC DENTAL IMPLANT PACK II is the device name listed in this FDA 510(k) record. The listed applicant is Ace Surgical Supply Co., Inc.. It received FDA 510(k) clearance on 1994-01-10 under 510(k) number K922649. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE BASIC DENTAL IMPLANT PACK II?

ACE BASIC DENTAL IMPLANT PACK II is a medical device that received FDA 510(k) clearance on 1994-01-10. The listed applicant is Ace Surgical Supply Co., Inc.. The 510(k) number is K922649.

When did ACE BASIC DENTAL IMPLANT PACK II receive FDA 510(k) clearance?

ACE BASIC DENTAL IMPLANT PACK II received FDA 510(k) clearance on 1994-01-10, under 510(k) number K922649.

Who is the listed applicant for ACE BASIC DENTAL IMPLANT PACK II?

The FDA 510(k) record lists Ace Surgical Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACE BASIC DENTAL IMPLANT PACK II?

The FDA product code for ACE BASIC DENTAL IMPLANT PACK II is EIA.

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 Ace Surgical Supply Co., 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 21 devices →

Related Devices (Code: EIA)

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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