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FDA 510(k)

EXPANDACELL INSTRUMENT WIPE

K-Number: K960621 · 1996-04-01

ApplicantShippert Medical Technologies Corp.
Decision Date1996-04-01
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EXPANDACELL INSTRUMENT WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Shippert Medical Technologies Corp.. It received FDA 510(k) clearance on 1996-04-01 under 510(k) number K960621. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPANDACELL INSTRUMENT WIPE?

EXPANDACELL INSTRUMENT WIPE is a medical device that received FDA 510(k) clearance on 1996-04-01. The listed applicant is Shippert Medical Technologies Corp.. The 510(k) number is K960621.

When did EXPANDACELL INSTRUMENT WIPE receive FDA 510(k) clearance?

EXPANDACELL INSTRUMENT WIPE received FDA 510(k) clearance on 1996-04-01, under 510(k) number K960621.

Who is the listed applicant for EXPANDACELL INSTRUMENT WIPE?

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

What is the FDA product code for EXPANDACELL INSTRUMENT WIPE?

The FDA product code for EXPANDACELL INSTRUMENT WIPE is GEC.

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Other records listing Shippert Medical Technologies 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.

K102117TISSU TRANS FILTRON SYRINGE FILLK092482TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500K092022TISSU TRANS HARVEST TUBINGK050797TISSU-TRANSK964855EXPANDACELL EYE SPEAR, EYE WICK, WICK DRAIN AND CORNEAL SHIELDK964334EXPANDACELL ANTI-FOG INSTRUMENT WIPE (WITH ALCOHOL)/(WITHOUT)

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Related Devices (Code: GEC)

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.

K971473IVALON INSTRUMENT WIPE, IVALON KNIFE CLEANING BLOCKM-Pact Worldwide Management Corp.K900691BIODYNE INSTRUMENT WIPESBio-Dyne, Inc.K896085SURGI-BRUSHSparta Surgical Corp.K875033STERILE SCRUBBY SCRUB BRUSHMedsurg Industries, Inc.K875129STERI-CLENSAbsorbent Cotton Co., Inc.K872823DELTA SCRUBPacific Biosystems, 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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