Atlas FDA

ACCOR MATRIX

FDA 510(k) clearance K790633 · decided 1979-05-17

Clearance details

K-number
K790633
Device name
ACCOR MATRIX
Applicant
Accor, Inc.
Decision
Substantially Equivalent
Date received
1979-04-03
Decision date
1979-05-17
Days to decision
44 days
Clearance type
Traditional
Product code
DZN
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Accor

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
COMPOTHIXO (K111465)Kerrhawe SA2012-07-25
DENTAL MATRIX BAND (K071858)Fly Cast Technologies, Inc.2007-08-31
CONTACT MOLAR BANDS AND CONTOUR STRIPS (K901919)Ivoclar North America, Inc.1990-06-22
CENTRIX PCR MOLAR MATRIX FORMS (BANDS) (K861581)Centrix, Inc.1986-05-12
TIGER BAND (K844324)World Wide Outdoor Marketing1984-12-03
INTERDENTAL WEDGES (K840984)Healthco, Inc.1984-04-13
DENTAL MATRIX BAND (K822094)Dentsply Intl.1982-08-16
COLORED WEDGE USED TO SEPARATE TEETH (K821444)Moyco Industries, Inc.1982-06-14
PALODENT MATRICES & BITINE RINGS (K801142)Alvin Meyer, D.D.S.1980-08-07
COREFORM MOLDS (K801530)Sybron Corp.1980-07-28
HEMO-WEDGE (K790555)Parker Laboratories, Inc.1980-01-17
RUWA MATRIX STRIPS (K790599)Howmedica Corp.1979-05-21

Recalls involving this device

No recalls on record reference this clearance.