FDA 510(k)

ZERO-G

K-Number: K842120 · 1984-06-08

Decision Date1984-06-08

Product CodeKIC

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ZERO-G is the device name listed in this FDA 510(k) record. The listed applicant is Steridyne Corp.. It received FDA 510(k) clearance on 1984-06-08 under 510(k) number K842120. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZERO-G?

ZERO-G is a medical device that received FDA 510(k) clearance on 1984-06-08. The listed applicant is Steridyne Corp.. The 510(k) number is K842120.

When did ZERO-G receive FDA 510(k) clearance?

ZERO-G received FDA 510(k) clearance on 1984-06-08, under 510(k) number K842120.

Who is the listed applicant for ZERO-G?

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

What is the FDA product code for ZERO-G?

The FDA product code for ZERO-G is KIC.

Other records listing Steridyne 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.

K925352CLEAN CUFF BLOOD PRESSURE CUFF LINER K911843ZERO-G(TM) GEL/FOAM MATTRESS TOPPER K911269MERCURY AND GLASS FEVER THERMOMETER K821314FEVER METER K801458WINTER HEAD DRESSING

Related Devices (Code: KIC)

K960189GEL-T CUSHIONSpan-America Medical Systems, Inc.K953352PROTEAM CUSHIONIskra.Med K954117CUSTOMCARE SEATING SYSTEMSpan-America Medical Systems, Inc.K950085MULTICURE(R) S GEL PADMultigestion (Deutschland) GmbH K945667MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHIONMicos Medical Systems K941858GEL CUSHIONHollister, Inc.

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.