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FDA 510(k)

SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL

K-Number: K950822 · 1995-03-22

ApplicantSolopak Laboratories, Inc.
Decision Date1995-03-22
Product CodeLDH
DecisionSubstantially Equivalent

Device Summary

SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL is the device name listed in this FDA 510(k) record. The listed applicant is Solopak Laboratories, Inc.. It received FDA 510(k) clearance on 1995-03-22 under 510(k) number K950822. The device is classified under product code LDH. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL?

SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL is a medical device that received FDA 510(k) clearance on 1995-03-22. The listed applicant is Solopak Laboratories, Inc.. The 510(k) number is K950822.

When did SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL receive FDA 510(k) clearance?

SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL received FDA 510(k) clearance on 1995-03-22, under 510(k) number K950822.

Who is the listed applicant for SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL?

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

What is the FDA product code for SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL?

The FDA product code for SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL is LDH.

Related Clinical Trials

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Related Devices (Code: LDH)

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.

K883686STERILE EMPTY GLASS VIALSFarris Laboratories, Inc.K875227STERILE EMPTY VIALSAllertech, Inc.

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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