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FDA 510(k)

COMPACT SYSTEM

K-Number: K790741 · 1979-04-26

ApplicantPausch Corp.
Decision Date1979-04-26
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPACT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pausch Corp.. It received FDA 510(k) clearance on 1979-04-26 under 510(k) number K790741. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPACT SYSTEM?

COMPACT SYSTEM is a medical device that received FDA 510(k) clearance on 1979-04-26. The listed applicant is Pausch Corp.. The 510(k) number is K790741.

When did COMPACT SYSTEM receive FDA 510(k) clearance?

COMPACT SYSTEM received FDA 510(k) clearance on 1979-04-26, under 510(k) number K790741.

Who is the listed applicant for COMPACT SYSTEM?

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

What is the FDA product code for COMPACT SYSTEM?

The FDA product code for COMPACT SYSTEM is KPR.

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Other records listing Pausch 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.

K973864COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMOK973834CS2000 & CS2000 TOMOK903395UROMAT 2000K870856COSMOSK790742KS-78 VERTICAL WALL CASSETTE HOLDERK790740BS 66, UNIVERSAL BUCKY STAND

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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