FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SNYDER DEBRIBEMENT SYSTEM LDP-1

K Number: K821321 · Decision Aug 6, 1982
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
16
Review Days
94

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SNYDER DEBRIBEMENT SYSTEM LDP-1
K Number
K821321
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Snyder Laboratories, Inc.
Date Received
May 4, 1982
Decision Date
August 6, 1982
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BTA), ordered by most recent decision date.

View all

Other Clearances by Snyder Laboratories, Inc.

K Number Device Name
K843906 SNYDER HEMOVAC WOUND DRAINAGE DEVICES
K800861 SNYDER HEMOVAC CHEST DRAINAGE SOLUTION
K800543 SNYDER HYSTERECTOMY Y TUBE KIT
K800577 SNYDER HEMOVAC TM VENTED WOUND KIT
K800578 SURGIVAC TM
K800542 100 ML SNYDER HEMOVAC
K790607 GREENLINE IRRIGATION TRAYS
K790606 CATHETERS, GREENLINE SUCTION
K790420 SUCTION CONNECTING TUBING
K790419 YANKAUER & POODLE SUCTION INSTRUMENTS
Search all 16 clearances from Snyder Laboratories, Inc. →