Atlas FDA

VISISTAT SKIN STAPLING DEVICE

FDA 510(k) clearance K844837 · decided 1985-01-23

Clearance details

K-number
K844837
Device name
VISISTAT SKIN STAPLING DEVICE
Applicant
Edward Weck, Inc.
Decision
Substantially Equivalent
Date received
1984-12-12
Decision date
1985-01-23
Days to decision
42 days
Clearance type
Traditional
Product code
GDT
Device class
1
Regulation number
878.4760
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Research Triangle Pa, NC, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
STAPLE REMOVAL KIT (K963234)Continental Medical Laboratories, Inc.1996-10-21
VISISTAT STAPLER (K943719)Pilling Weck, Inc.1994-08-24
MANIPLER DISPOSABLE SKIN STAPLER (K925526)Matsutani Seisakusho Co. , Ltd.1993-06-24
SKIN STAPLE REMOVER KIT (K915430)Cypress Medical Products, Ltd.1992-02-28
QUALTEX SKIN STAPLE EXTRACTOR (K911204)Deroyal Industries, Inc.1991-05-08
AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER* (K910586)United States Surgical, A Division of Tyco Healthc1991-03-07
APPOSE UNITY STERILE DISPOSABLE SKIN STAPLER (K900486)Davis & Geck, Inc.1990-04-20
SKIN STAPLE REMOVER WITH SPONGE STERILE DISPOSABLE (K861711)Busse Hospital Disposables, Inc.1986-05-16
V. MUELLER VITAL SKIN STAPLER (K851974)American V. Mueller1985-06-11
SKIN STAT II SKIN STAPLING MEDICAL DEVICE (K844838)Edward Weck, Inc.1985-01-23
STAPLE REMOVER SR300P (K833085)Prosper, Inc.1984-12-14
VYDAX 525-550 & 5100 FLUOROTELOMER (K833357)ETHICON, Inc.1983-12-12

Recalls involving this device

No recalls on record reference this clearance.