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FDA 510(k)

VOLU-SOL URINARY SEDIMENT STAIN

K-Number: K792495 · 1979-12-18

Decision Date1979-12-18
Product CodeICF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VOLU-SOL URINARY SEDIMENT STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1979-12-18 under 510(k) number K792495. The device is classified under product code ICF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLU-SOL URINARY SEDIMENT STAIN?

VOLU-SOL URINARY SEDIMENT STAIN is a medical device that received FDA 510(k) clearance on 1979-12-18. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K792495.

When did VOLU-SOL URINARY SEDIMENT STAIN receive FDA 510(k) clearance?

VOLU-SOL URINARY SEDIMENT STAIN received FDA 510(k) clearance on 1979-12-18, under 510(k) number K792495.

Who is the listed applicant for VOLU-SOL URINARY SEDIMENT STAIN?

The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOLU-SOL URINARY SEDIMENT STAIN?

The FDA product code for VOLU-SOL URINARY SEDIMENT STAIN is ICF.

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 Volu Sol Medical Industries 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 66 devices →

Related Devices (Code: ICF)

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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