Matheson Gas Products, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Matheson Gas Products, Inc.” (first 1987, latest 1988), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 32 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
BXKGas, Calibration (Specified Concentration)44
GEXPowered Laser Surgical Instrument11

Review panels

Most recent Matheson Gas Products, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K882516THREE-COMPONENT MEDICAL LASER GAS MIXTURESGEX1988-08-0344
K871100O.1 TO 25.0% CARB. DIOX. U.S.P. BALANCE OXYGEN USPBXK1987-04-2133
K871103O.1 T0 40.0% CARBON DIOX. O.1 TO 90.0% OXY. U.S.PBXK1987-04-2032
K871102O.1 TO 50.0% CARBON DIOXIDE, USP BALANCE NITRO.,NFBXK1987-04-2032
K8711010.1 TO 25.0% OXYGEN, USP, BALANCE NITROGEN, N.F.BXK1987-04-2032

Recalls

openFDA lists no recalls under a recalling firm named Matheson Gas Products, 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 Matheson Gas Products, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Matheson Gas Products, Inc.” (first 1987, latest 1988), across 2 product codes in 2 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 Matheson Gas Products, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Matheson Gas Products, Inc. is 32 days.

Which FDA product codes appear under Matheson Gas Products, Inc.?

The most frequent FDA product codes under this applicant name are BXK (Gas, Calibration (Specified Concentration), 4); GEX (Powered Laser Surgical Instrument, 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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