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FDA 510(k)

PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN

K-Number: K892673 · 1989-05-31

Decision Date1989-05-31
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN is the device name listed in this FDA 510(k) record. The listed applicant is T.C. Electronics Co.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K892673. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN?

PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is T.C. Electronics Co.. The 510(k) number is K892673.

When did PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN received FDA 510(k) clearance on 1989-05-31, under 510(k) number K892673.

Who is the listed applicant for PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN?

The FDA 510(k) record lists T.C. Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN?

The FDA product code for PATIENT EXAM GLOVES (VINYL) MFG. PRECIOUS MOUNTAIN is LYZ.

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 T.C. Electronics Co. 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.

Related Devices (Code: LYZ)

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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