Plasmedics, Inc.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Plasmedics, Inc.” (first 1982, latest 1985), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 86 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
BZQMonitor, Breathing Frequency22
BSJMask, Gas, Anesthetic11
DYGCatheter, Flow Directed11
FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days11

Plus 1 more product codes.

Review panels

Most recent Plasmedics, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K853559STERILE BIOPSY NEEDLES—1985-09-1116
K850263PEDIATRIC ANESTHESIA MASK W/PACIFIER/RING ASSEMBLYBSJ1985-03-2561
K831601APNEA ALARM FOR ADULT-PEDIATRIC & NEONBZQ1983-09-26131
K831650ANESTHESIA/RESPIRATORY DISCONNECT -BZQ1983-09-12112
K830604WEDGE PRESSURE CATHETERDYG1983-07-18143
K823351CENTRAL VENOUS CATHETERFOZ1982-12-0930

Recalls

openFDA lists no recalls under a recalling firm named Plasmedics, Inc..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Plasmedics, Inc.?

FDA lists 6 510(k) clearances under the applicant name “Plasmedics, Inc.” (first 1982, latest 1985), across 5 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Plasmedics, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Plasmedics, Inc. is 86 days.

Which FDA product codes appear under Plasmedics, Inc.?

The most frequent FDA product codes under this applicant name are BZQ (Monitor, Breathing Frequency, 2); BSJ (Mask, Gas, Anesthetic, 1); DYG (Catheter, Flow Directed, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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