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FDA 510(k)

COSMOS

K-Number: K870856 · 1987-03-30

ApplicantPausch Corp.
Decision Date1987-03-30
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COSMOS is the device name listed in this FDA 510(k) record. The listed applicant is Pausch Corp.. It received FDA 510(k) clearance on 1987-03-30 under 510(k) number K870856. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COSMOS?

COSMOS is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Pausch Corp.. The 510(k) number is K870856.

When did COSMOS receive FDA 510(k) clearance?

COSMOS received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870856.

Who is the listed applicant for COSMOS?

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 COSMOS?

The FDA product code for COSMOS is IYB.

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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 2000K790740BS 66, UNIVERSAL BUCKY STANDK790741COMPACT SYSTEMK790742KS-78 VERTICAL WALL CASSETTE HOLDER

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Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, Inc.

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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