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FDA 510(k)

SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700

K-Number: K920986 · 1992-06-04

ApplicantSnowden-Pencer
Decision Date1992-06-04
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700 is the device name listed in this FDA 510(k) record. The listed applicant is Snowden-Pencer. It received FDA 510(k) clearance on 1992-06-04 under 510(k) number K920986. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700?

SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700 is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Snowden-Pencer. The 510(k) number is K920986.

When did SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700 receive FDA 510(k) clearance?

SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700 received FDA 510(k) clearance on 1992-06-04, under 510(k) number K920986.

Who is the listed applicant for SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700?

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

What is the FDA product code for SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700?

The FDA product code for SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700 is HIF.

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Other records listing Snowden-Pencer 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.

K960400DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)K930666REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERYK930667REUSABLE LAPAROSCOPIC INSTRUMENTSK924148DIAMOND-SHARP(R) TROCARSK924149ENDO I/A PROBEK920985SNOWDEN-PENCER IRRIGATION PUMP

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Related Devices (Code: HIF)

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.

K260209ENDOFLATOR+; Smart Smoke EvacuationKarl Storz SE & CO. KGK252584Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)Weyo Surgical Technology , Ltd.K252318Insufflator (OPTO-IFL1000)Guangdong Optomedic Technologies, Inc.K250388ENDOFLATOR +Karl Storz SE & CO. KGK242772AirSurgN Insufflator (10030/AirSurgN)SmartsurgN, Inc.K243527High Flow Insufflation Unit (UHI-4)Olympus Medical Systems Corporation

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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