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FDA 510(k)

SNYDER HEMOVAC CHEST DRAINAGE SOLUTION

K-Number: K800861 · 1980-05-02

Decision Date1980-05-02
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SNYDER HEMOVAC CHEST DRAINAGE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Snyder Laboratories, Inc.. It received FDA 510(k) clearance on 1980-05-02 under 510(k) number K800861. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNYDER HEMOVAC CHEST DRAINAGE SOLUTION?

SNYDER HEMOVAC CHEST DRAINAGE SOLUTION is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K800861.

When did SNYDER HEMOVAC CHEST DRAINAGE SOLUTION receive FDA 510(k) clearance?

SNYDER HEMOVAC CHEST DRAINAGE SOLUTION received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800861.

Who is the listed applicant for SNYDER HEMOVAC CHEST DRAINAGE SOLUTION?

The FDA 510(k) record lists Snyder Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNYDER HEMOVAC CHEST DRAINAGE SOLUTION?

The FDA product code for SNYDER HEMOVAC CHEST DRAINAGE SOLUTION is KDQ.

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 Snyder Laboratories, 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 16 devices →

Related Devices (Code: KDQ)

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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