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FDA 510(k)

STERILE EMPTY GLASS VIALS

K-Number: K883686 · 1988-09-23

Decision Date1988-09-23
Product CodeLDH
DecisionSubstantially Equivalent

Device Summary

STERILE EMPTY GLASS VIALS is the device name listed in this FDA 510(k) record. The listed applicant is Farris Laboratories, Inc.. It received FDA 510(k) clearance on 1988-09-23 under 510(k) number K883686. The device is classified under product code LDH. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE EMPTY GLASS VIALS?

STERILE EMPTY GLASS VIALS is a medical device that received FDA 510(k) clearance on 1988-09-23. The listed applicant is Farris Laboratories, Inc.. The 510(k) number is K883686.

When did STERILE EMPTY GLASS VIALS receive FDA 510(k) clearance?

STERILE EMPTY GLASS VIALS received FDA 510(k) clearance on 1988-09-23, under 510(k) number K883686.

Who is the listed applicant for STERILE EMPTY GLASS VIALS?

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

What is the FDA product code for STERILE EMPTY GLASS VIALS?

The FDA product code for STERILE EMPTY GLASS VIALS is LDH.

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.

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.

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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