FDA 510(k)

LIFEPORT II, MODEL LPS-1100

K-Number: K881075 · 1988-06-03

Decision Date1988-06-03

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LIFEPORT II, MODEL LPS-1100 is the device name listed in this FDA 510(k) record. The listed applicant is Strato Medical Corp.. It received FDA 510(k) clearance on 1988-06-03 under 510(k) number K881075. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPORT II, MODEL LPS-1100?

LIFEPORT II, MODEL LPS-1100 is a medical device that received FDA 510(k) clearance on 1988-06-03. The listed applicant is Strato Medical Corp.. The 510(k) number is K881075.

When did LIFEPORT II, MODEL LPS-1100 receive FDA 510(k) clearance?

LIFEPORT II, MODEL LPS-1100 received FDA 510(k) clearance on 1988-06-03, under 510(k) number K881075.

Who is the listed applicant for LIFEPORT II, MODEL LPS-1100?

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

What is the FDA product code for LIFEPORT II, MODEL LPS-1100?

The FDA product code for LIFEPORT II, MODEL LPS-1100 is LJT.

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Other records listing Strato Medical Corp. as applicant

K945956STRATO MEDICAL INFUSE-A-CATH TRIPLE LUMEN SILICONE CATHETER SYSTEMS K946250STRATO MEDICAL INFUSE-A-CATH, TRIPLE LUMEN POLYURETHANE, CENTRAL VNOUS CATHETER SYSTEMS K942848STRATO MEDICAL LIFEPORT LPS 7515 K934518STRATO MEDICAL INFUSE-A-PORT/INFUSE-A-KIT PERIPORT PERIPHERAL ACCESS SYSTEM K932509STRATO MEDICAL INFUSE-A-PORT/SNAP-LOCK MACROPRORT K933884STRATO MEDICAL LIFEPORT LPS 7255 LOW PROFILE DUAL LUMEN VASCULAR ACCESS SYSTEM

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Related Devices (Code: LJT)

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Official Source

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