SOFCARE PATIENT EXAMINATION GLOVES (LATEX)
K-Number: K891965 · 1989-08-31
Advertisement
Device Summary
Frequently Asked Questions
What is the SOFCARE PATIENT EXAMINATION GLOVES (LATEX)?
SOFCARE PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is P. T. Tata Rubberindo Industries. The 510(k) number is K891965.
When did SOFCARE PATIENT EXAMINATION GLOVES (LATEX) receive FDA 510(k) clearance?
SOFCARE PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-08-31, under 510(k) number K891965.
Who is the listed applicant for SOFCARE PATIENT EXAMINATION GLOVES (LATEX)?
The FDA 510(k) record lists P. T. Tata Rubberindo Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOFCARE PATIENT EXAMINATION GLOVES (LATEX)?
The FDA product code for SOFCARE 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 P. T. Tata Rubberindo 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.
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.
Advertisement