Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ATS PVA FIXATIVE SOLUTION

K-Number: K881698 · 1988-05-13

Decision Date1988-05-13
Product CodeLDZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

ATS PVA FIXATIVE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Tec Systems, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K881698. The device is classified under product code LDZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATS PVA FIXATIVE SOLUTION?

ATS PVA FIXATIVE SOLUTION is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Alpha-Tec Systems, Inc.. The 510(k) number is K881698.

When did ATS PVA FIXATIVE SOLUTION receive FDA 510(k) clearance?

ATS PVA FIXATIVE SOLUTION received FDA 510(k) clearance on 1988-05-13, under 510(k) number K881698.

Who is the listed applicant for ATS PVA FIXATIVE SOLUTION?

The FDA 510(k) record lists Alpha-Tec Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATS PVA FIXATIVE SOLUTION?

The FDA product code for ATS PVA FIXATIVE SOLUTION is LDZ.

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 Alpha-Tec Systems, 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 18 devices →

Related Devices (Code: LDZ)

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.

↑