ClearanceBrief
Company ยท US

Cunningham Woodland, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1983. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LDQ4
DWSInstruments, Surgical, Cardiovascular1
FMFSyringe, Piston1
FSMTray, Surgical, Instrument1
GDYGauze/Sponge, Internal, X-Ray Detectable1
KDDKit, Surgical Instrument, Disposable1
KMEBedding, Disposable, Medical1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 31, 1983K823527SUBCLAVIAN INSERTION KIT
Cunningham Woodland, Inc.
FMF
Jan 22, 1982K813286PRE-PACK TENS
Cunningham Woodland, Inc.
GDY
Jan 5, 1982K813519NON-ABSORBENT TOWELS
Cunningham Woodland, Inc.
KME
Dec 29, 1981K813284VENOUS CANNULA TRAY
Cunningham Woodland, Inc.
DWS
May 8, 1981K811091MINOR DRESSING TRAY
Cunningham Woodland, Inc.
LDQ
May 8, 1981K811090MAJOR DRESSING TRAY
Cunningham Woodland, Inc.
LDQ
May 8, 1981K811089ONE STEP PREP KIT
Cunningham Woodland, Inc.
LDQ
May 8, 1981K811088DRESSING TRAY MERCY HOSPITAL
Cunningham Woodland, Inc.
LDQ
May 1, 1981K811087MIKA SKIN SCRUB TRAY PRE OPERATIVE W/GEL
Cunningham Woodland, Inc.
FSM
May 1, 1981K811086SUTURE REMOVAL SET(DISPLSABLE)
Cunningham Woodland, Inc.
KDD

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes