RUBBERCARE PATIENT EXAMINATION GLOVE— 510(k) K891123
Substantially EquivalentPerusahaan Pelindung Getah (M) Sdn Bhd
FDA 510(k) clearance K891123 for RUBBERCARE PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-07-14. Applicant: Perusahaan Pelindung Getah (M) Sdn Bhd. Device class: 1.
Clearance details
- Applicant
- Perusahaan Pelindung Getah (M) Sdn Bhd
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seremban, N.S., MY
Recent devices under product code LYY
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- K223298 — Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L)
- K222612 — Powder-Free Latex examination gloves
More clearances from Perusahaan Pelindung Getah (M) Sdn Bhd
view all- K072300 — POWDER FREE NATURAL RUBBER LOW MODULUS LATEX PATIENT EXAMINATION GLOVES WITH A PROTEIN LABELING CLAIM
- K032201 — RUBBERCARE POWDERED LATEX EXAMINATION GLOVES
- K002111 — RUBBERCARE POLYMER-COATED POWDERED LATEX EXAMINATION GLOVES/GUARDIAN POLYMER-COATED POWDERED EXAMINATION GLOVES. CONTAI
- K002112 — RUBBERCARE POLYMER-CHLORINATED POWDER-FREE GUARDIAN POLYMER-CHLORINATED POWDER-FREE
- K002114 — RUBBERCARE GUARDIAN POLYMER-COATED POWDER-FREE LATEX EXAMINATION GLOVES: CONTAINS 100 MICROGRAMS OR LESS OF TOTAL WATER
Data sourced from openFDA. This site is unofficial and independent of the FDA.