HEDY PATIENT EXAMINATION GLOVES (LATEX)
K-Number: K891671 · 1989-10-27
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Device Summary
Frequently Asked Questions
What is the HEDY PATIENT EXAMINATION GLOVES (LATEX)?
HEDY PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is Hedd Industry Corp.. The 510(k) number is K891671.
When did HEDY PATIENT EXAMINATION GLOVES (LATEX) receive FDA 510(k) clearance?
HEDY PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-10-27, under 510(k) number K891671.
Who is the listed applicant for HEDY PATIENT EXAMINATION GLOVES (LATEX)?
The FDA 510(k) record lists Hedd Industry Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEDY PATIENT EXAMINATION GLOVES (LATEX)?
The FDA product code for HEDY PATIENT EXAMINATION GLOVES (LATEX) is LYY.
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 Hedd Industry Corp. 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: LYY)
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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