Guthrie Medicare Products (Melaka) Sdn Bhd
Great Neck, NY, US
Guthrie Medicare Products (Melaka) Sdn Bhd appears in FDA device records in Great Neck, NY. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Guthrie Medicare Products (Melaka) Sdn Bhd between 1991 and 2001. The busiest year on record is 2001, with 5. The most recent is 2001, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 1 |
| 1996 | 1 |
| 1999 | 1 |
| 2000 | 4 |
| 2001 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K003922 | NITRILE EXAMINATION GLOVES (POWERED) | LZA | Substantially Equivalent | |
| K003985 | POWDERFREE NITRILE PATIENT EXMINATION GLOVE | LZA | Substantially Equivalent | |
| K010078 | GUTHRIE SHIELD PLUS BLUE LATEX EXAMINATION GLOVES (POWDER-FREE) | LYY | Substantially Equivalent | |
| K010054 | GUTHRIE SHIELD BLUE LATEX EXAMINATION GLOVES, POWDERED WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS) | LYY | Substantially Equivalent | |
| K003872 | GUTHRIE PRIME POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS) | LYY | Substantially Equivalent | |
| K001049 | GUTHRIE POWDER-FREE LATEX SURGICAL GLOVE WITH (50 MICROGRAMS OR LESS) | KGO | Substantially Equivalent | |
| K001047 | GUTHRIE LATEX SURGICAL GLOVE (PRE-POWDERED) | KGO | Substantially Equivalent | |
| K000090 | GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K993793 | GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K990228 | GUTHRIE PRIME POWDER-FREE | LYY | Substantially Equivalent | |
| K954967 | GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K911694 | PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) | LYY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Guthrie Medicare Products (Melaka) Sdn Bhd edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Guthrie Medicare Products (Melaka) Sdn Bhd. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain