Atlas FDA

SCALPEL HANDLE

FDA 510(k) clearance K854858 · decided 1985-12-24

Clearance details

K-number
K854858
Device name
SCALPEL HANDLE
Applicant
Medelec Intl. Corp.
Decision
Substantially Equivalent
Date received
1985-12-05
Decision date
1985-12-24
Days to decision
19 days
Clearance type
Traditional
Product code
GDZ
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Miami Beach, FL, 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
SPECTRA MEDICAL SAFETY SCAPEL (K091462)Spectra, Inc.2009-12-15
SCALPEL HANDLE (K890242)Kinetic Medical Products1989-01-27
BEAVER(R) HANDLE (K884512)Bd Becton Dickinson Vacutainer Systems Preanalytic1988-11-17
P.S.I.-DISPOSABLE SCALPEL SURGEONS HANDLE (K863951)Precision Surgical Industries, Inc.1986-10-24
THE S. CORDERO STYLUS (K863808)S. Cordero Co.1986-10-14
KEISEI HANDLES FOR SURGICAL BLADES (K863212)Keisei Medical Industrial Co., Ltd.1986-09-02
SCALPEL HANDLE #7 SS 410 OR 420 (K852735)The Huxley Instrument Corp.1985-07-15
SCALPEL HANDLE #3 SS 410 OR 420 (K852711)The Huxley Instrument Corp.1985-07-15
7-103, 7-104, 7-107 SCALPEL HANDLES, #3 #4 #7 (K851750)Artiberia1985-06-20
BRIMFIELD CANNULATED BLADE HOLDER (K852042)Brimfield Scientific Instruments1985-06-11
SURGICAL PAWS (K812876)M-W Laboratories, Inc.1981-11-20
ZEE SURGICAL INSTRUMENTS (K812814)Zee Medical Products Co., Inc.1981-11-06

Recalls involving this device

No recalls on record reference this clearance.