Atlas FDA

CONPHAR PERCUSSION HAMMER(TAYLOR)

FDA 510(k) clearance K803148 · decided 1981-01-08

Clearance details

K-number
K803148
Device name
CONPHAR PERCUSSION HAMMER(TAYLOR)
Applicant
Conphar, Inc.
Decision
Substantially Equivalent
Date received
1980-12-12
Decision date
1981-01-08
Days to decision
27 days
Clearance type
Traditional
Product code
GWZ
Device class
1
Regulation number
882.1700
Medical specialty
Neurology
Advisory committee
Neurology
Location
Mchenry, IL, 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
PERCUSSION HAMMER (K891571)Sandal Surgico1989-03-31
TAYLOR PERCUSSION HAMMER SS 410 OR 420 (K852716)The Huxley Instrument Corp.1985-07-26
1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE (K851748)Artiberia1985-06-13
H.R. JAKOBI SURG. INSTR. #10 34/36 (K834178)Imm Enterprises , Ltd.1984-02-23
CAT 10-NEUROLOGY DEVICE (K840314)Imm Enterprises , Ltd.1984-02-23
OP-CON SURG. INSTRUMENT #10 (K834170)Imm Enterprises , Ltd.1984-02-23
RICA (DIAGNOSTIC INSTRUMENTS) (K810054)Robert I. Chien & Assoc., Inc.1981-01-28
CONPHAR PERCUSSION HAMMER(BUCK TYPE) (K803174)Conphar, Inc.1980-12-30
TAYLOR NEUROLOGICAL HAMMER (K791337)Amdia Medical Products1979-08-03
BUCKS NEUROLOGICAL HAMMER (K791336)Amdia Medical Products1979-08-03

Recalls involving this device

No recalls on record reference this clearance.