Pajunk GmbH
Pajunk GmbH holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2012, with 1 FDA device recall on record.
Top product codes for Pajunk GmbH
FDA recalls by Pajunk GmbH
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Pajunk GmbH
- K113207 — SONO TAP, TUOHY SONO
- K113209 — CHIBA SONO
- K060563 — EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IV
- K053283 — UNIPLEX NANOLINE CANNULA, PLEXOLONG NANOLINE SET, STIMULONG NANOLINE SET
- K053282 — ADAPTABLE MONOPOLAR ELECTRODES WITH CERAMIC TIP
- K042979 — MODIFICATION TO: PLEXALONG SETS
- K043130 — MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS
- K040965 — PAJUNK TUOHY NEEDLES, QUINCKE NEEDLES, CHIBA NEEDLES & CRAWFORD NEEDLES
- K033018 — STIMULONG PLUS CATHETER SET MODEL, VARIOUS
- K033249 — PAJUNK MODULAR HANDLE INSTRUMENTS
- K023218 — MODIFICATION TO PLEXOLONG SETS
- K013041 — PLEXOLONG SETS
- K011308 — MULTISTIM
- K012771 — TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX
- K011997 — MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX
- K000722 — UNIPOLAR NEEDLES
- K911221 — ATRAUMATIC SPECIAL SPROTTE NEEDLE
- K911202 — ATRAUMATIC STANDARD SPROTTE NEEDLE
- K911260 — ATRAUMATIC STANDARD SPROTTE NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.