FDA 510(k)

SQUEEZE PLAY

K-Number: K943730 · 1994-11-28

Decision Date1994-11-28

Product CodeIRO

Advisory CommitteePM

DecisionSubstantially Equivalent for Some Indications

Device Summary

SQUEEZE PLAY is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K943730. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SQUEEZE PLAY?

SQUEEZE PLAY is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Conair Corp.. The 510(k) number is K943730.

When did SQUEEZE PLAY receive FDA 510(k) clearance?

SQUEEZE PLAY received FDA 510(k) clearance on 1994-11-28, under 510(k) number K943730.

Who is the listed applicant for SQUEEZE PLAY?

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

What is the FDA product code for SQUEEZE PLAY?

The FDA product code for SQUEEZE PLAY is IRO.

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Other records listing Conair Corp. as applicant

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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.