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FDA 510(k)

CD-102 CARBON DIOXIDE ANALYZER/RECOR

K-Number: K833739 · 1983-12-16

ApplicantInstrumentarium Corp.
Decision Date1983-12-16
Product CodeCCJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CD-102 CARBON DIOXIDE ANALYZER/RECOR is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Corp.. It received FDA 510(k) clearance on 1983-12-16 under 510(k) number K833739. The device is classified under product code CCJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CD-102 CARBON DIOXIDE ANALYZER/RECOR?

CD-102 CARBON DIOXIDE ANALYZER/RECOR is a medical device that received FDA 510(k) clearance on 1983-12-16. The listed applicant is Instrumentarium Corp.. The 510(k) number is K833739.

When did CD-102 CARBON DIOXIDE ANALYZER/RECOR receive FDA 510(k) clearance?

CD-102 CARBON DIOXIDE ANALYZER/RECOR received FDA 510(k) clearance on 1983-12-16, under 510(k) number K833739.

Who is the listed applicant for CD-102 CARBON DIOXIDE ANALYZER/RECOR?

The FDA 510(k) record lists Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CD-102 CARBON DIOXIDE ANALYZER/RECOR?

The FDA product code for CD-102 CARBON DIOXIDE ANALYZER/RECOR is CCJ.

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Other records listing Instrumentarium Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K022630MODIFICATION TO FOCUSK001729FOCUSK001439ORTHOCEPH OC100 DK992385ORTHOPANTOMOGRAPH OP100DK981641MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQK962638TONOCAP, TC-200 AND ACCESSORY CATHETERS

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Related Devices (Code: CCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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