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FDA 510(k)

SCRATCH & SNIFF FOR ANESTHESIA

K-Number: K840431 · 1984-05-14

ApplicantDryden Corp.
Decision Date1984-05-14
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SCRATCH & SNIFF FOR ANESTHESIA is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1984-05-14 under 510(k) number K840431. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCRATCH & SNIFF FOR ANESTHESIA?

SCRATCH & SNIFF FOR ANESTHESIA is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Dryden Corp.. The 510(k) number is K840431.

When did SCRATCH & SNIFF FOR ANESTHESIA receive FDA 510(k) clearance?

SCRATCH & SNIFF FOR ANESTHESIA received FDA 510(k) clearance on 1984-05-14, under 510(k) number K840431.

Who is the listed applicant for SCRATCH & SNIFF FOR ANESTHESIA?

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

What is the FDA product code for SCRATCH & SNIFF FOR ANESTHESIA?

The FDA product code for SCRATCH & SNIFF FOR ANESTHESIA is CAI.

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Other records listing Dryden 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.

K880923PATIENT VENTILATOR ISOLATORK880769BREATHING CIRCUIT W/HEATED WIREK882285NONREBREATHING CIRCUITK873928UNIVERSAL TOURNIQUETK873927REUSEABLE BREATHING TUBESK870859BAG-TAIL BLEED VALVE

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Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, 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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